Dual molecular delivery of oligonucleotides and peptide containing conjugates

ABSTRACT

Disclosed herein is a method for inhibiting expression of a gene of a subject comprising administering (1) a composition comprising R-(L) a -(G) b ; wherein R is an oligonucleotide selected from the group consisting of DNA, RNA, siRNA, and microRNA; L is a linker and each occurance of L is independently selected from Table 3; G is a targeting ligand and each occurance of G is independently selected from Table 4; each of a and b is independently 0, 1, 2, 3 or 4; and (2) a composition comprising (P) c -(L) d -(G) e ; wherein P is a peptide and each occurance of P is independently selected from Table 2; L is a linker and each occurance of L is independently selected from Table 3; G is a targeting ligand and each occurance of G is independently selected from Table 4; d is 0, 1, 2, 3, 4, 5 or 6; and each of c and e is independently 1, 2, 3, 4, 5 or 6. Compositions in (1) and (2) can be co-administered or sequentially administered.

BACKGROUND OF THE INVENTION

The delivery of oligonucleotides and other cell membrane impermeable compounds into a living cell is highly restricted by the complex membrane system of the cell. Drugs used in antisense, RNAi, and gene therapies are relatively large hydrophilic polymers and are frequently highly negatively charged. These physical characteristics severely restrict their direct diffusion across the cell membrane. For this reason, the major barrier to polynucleotide therapeutic efficacy is the delivery of the polynucleotide across a cell membrane to the cell cytoplasm or nucleus.

One approach that has been used to deliver small nucleic acid in vivo has been to attach the nucleic acid to either a small targeting molecule or a lipid or sterol. While some delivery and activity has been observed with these conjugates, the very large nucleic acid dose required with these methods is impractical.

Considerable amount of literature evidence supports the hypothesis that the major hurdles for oligonucleotide delivery are cell uptake and endosomal escape. Small interfering RNAs (siRNA) can achieve selective knock-down of therapeutic targets by degradation of specific messenger RNA, provided the siRNA reaches the RNA Induced Silencing Complex (RISC) in the cell cytosol. Receptor-targeted siRNA constructs can be taken up by cell surface receptors and accumulate in subcellular vesicles termed endosomes. A small fraction of the siRNA traverses the endosomal membrane to reach the cytosol. The process, termed endosomal escape, is a major barrier to cytosolic delivery and higher potency of siRNA therapeutics.

There remains a need for additional compositions or or delivery methods that can provide effective in vivo delivery, cell uptake and/or endosomal escape of oligonucleotides.

SUMMARY OF THE INVENTION

The compositions and administration methods disclosed herein provide unexpected effective in vivo delivery of an oligonucleotide through dual molecular delivery of the oligonucleotide and a peptide containing conjugate which are not covalently linked to each other.

One embodiment includes a method for inhibiting expression of a gene of a subject comprising administering (1) a composition comprising R-(L)_(a)-(G)_(b) to the subject; wherein R is an oligonucleotide with the ability to inhibit expression of a gene; L is a linker and each occurance of L is independently selected from Table 3; G is a targeting ligand and each occurance of G is independently selected from Table 4; each of a and b is independently 0, 1, 2, 3 or 4; and (2) a composition comprising (P)_(c)-(L)_(d)-(G)_(e) to the subject; wherein P is a peptide and each occurance of P is independently selected from Table 2; L is a linker and each occurance of L is independently selected from Table 3; G is a targeting ligand and each occurance of G is independently selected from Table 4; d is 0, 1, 2, 3, 4, 5 or 6; and each of c and e is independently 1, 2, 3, 4, 5 or 6. In one embodiment, R is an oligonucleotide selected from the group consisting of DNA, RNA, siRNA, and microRNA.

In one embodiment, a method for expressing a protein or polypeptide in a subject comprises administering: (1) a composition comprising R-(L)_(a)-(G)_(b) to the subject; wherein R is an oligonucleotide with the ability to encode a protein or polypeptide; L is a linker and each occurance of L is independently selected from Table 3; G is a targeting ligand and each occurance of G is independently selected from Table 4; each of a and b is independently 0, 1, 2, 3 or 4; and (2) a composition comprising (P)_(c)-(L)_(d)-(G)_(e) to the subject; wherein P is a peptide and each occurance of P is independently selected from Table 2; L is a linker and each occurance of L is independently selected from Table 3; G is a targeting ligand and each occurance of G is independently selected from Table 4; d is 0, 1, 2, 3, 4, 5 or 6; and each of c and e is independently 1, 2, 3, 4, 5 or 6. In one embodiment, R is an oligonucleotide selected from the group consisting of DNA, RNA, and mRNA.

In one embodiment, a composition for dual molecular delivery of an oligonucleotide and a peptide conjugate comprises (1) R-(L)_(a)-(G)_(b); and (2) (P)_(c)-(L)_(d)-(G)_(e); wherein R is an oligonucleotide with the ability to inhibit expression of a gene; P is a peptide and each occurance of P is independently selected from Table 2; L is a linker and each occurance of L is independently selected from Table 3; G is a targeting ligand and each occurance of G is independently selected from Table 4; each of a and b is independently 0, 1, 2, 3 or 4; d is 0, 1, 2, 3, 4, 5 or 6; and each of c and e is independently 1, 2, 3, 4, 5 or 6. In one embodiment, R is an oligonucleotide selected from the group consisting of DNA, RNA, siRNA, and microRNA

In one embodiment, a composition for dual molecular delivery of an oligonucleotide and a peptide conjugate comprises (1) R-(L)_(a)-(G)_(b); and (2) (P)_(c)-(L)_(d)-(G)_(e); wherein R is an oligonucleotide with the ability to encode a protein or polypeptide; P is a peptide and each occurance of P is independently selected from Table 2; L is a linker and each occurance of L is independently selected from Table 3; G is a targeting ligand and each occurance of G is independently selected from Table 4; each of a and b is independently 0, 1, 2, 3 or 4; d is 0, 1, 2, 3, 4, 5 or 6; and each of c and e is independently 1, 2, 3, 4, 5 or 6. In one embodiment, R is an oligonucleotide selected from the group consisting of DNA, RNA, and mRNA.

In one embodiment, the composition comprises R-(L)_(a)-(G)_(b) and the composition comprising (P)_(c)-(L)_(d)-(G)_(e) are co-administered to the subject at the same time. In one embodiment, the composition comprising R-(L)_(a)-(G)_(b) and the composition comprising (P)_(c)-(L)_(d)-(G)_(e) are sequentially administered to the subject about 5 to 60 minutes apart.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a time course of mRNA KD following different treatments. Sequential dosing with peptide (or sucrose buffer) was dosed 15 min after siRNA. The 5 mg/kg siRNA only group had no peptide or sucrose buffer and was dosed s.c. compared to all other groups dosed via i.v. route. FIG. 1 shows both peptides generated faster mRNA knockdown (KD) compared to siRNA alone (dose matched by i.v. or standard SCE format by s.c.).

FIG. 2 shows a time course of RISC loading following different treatments. RISC data which shows faster RISC loading for both peptides matches the mRNA KD data. At 72 hr, there is 10 to 20-fold higher RISC loading with DMD compared to 0.5 mg/kg dose of siRNA with buffer (no peptide). With DMD format, there is 3 to 4-fold higher RISC loading compared to a 10× higher dose with standard subQ siRNA format.

FIG. 3 shows liver siRNA PK. This figure indicates peptide does not influence amount of siRNA in liver over time. It also shows that s.c. injection of 10-fold higher siRNA dose gets more siRNA into liver. DMD can achieve greater RISC loading and mRNA KD with less siRNA in liver.

FIG. 4 shows a time course of mRNA KD following different treatments. Sequential dosing with peptide (or sucrose buffer) dosed 15 min after siRNA. This figure shows that addition of vinylPmoeT to GS (siRNA-III) generates faster KD compared to siRNA-I. Both siRNAs show faster and greater KD in DMD format compared to 5-fold higher dose of siRNA-III alone.

FIG. 5 shows a time course of RISC loading following different treatments. This data matches the mRNA KD data, showing the siRNA-III generates faster RISC loading due to addition of vinyl phosphonate. It also shows the rate of RISC loading is much faster when using peptides in DMD format compared to siRNA alone.

FIG. 6 shows a time course of RISC loading following different treatments. The order of siRNA stability is siRNA-I>siRNA-V>siRNA-VI and the data shows that metabolic stability is critical to siRNA activity. With a highly stable siRNA-I, the timing of peptide dose does not significantly change the activity (within 2 hr before up to 24 hr after siRNA dose). With the moderately stable siRNA-V, peptide dose times within 2 hr (before or after) the siRNA generate a low level of activity (˜25% KD). Longer separation times (4-24 hr post-siRNA dose) or more unstable siRNAs (siRNA-VI) both reduced the activity to background levels.

FIG. 7 shows mRNA KD in monkey liver. The mRNA expression relative to each animal's pre-dose biopsy. Achieved ˜50% KD in non-human primates at 10 mpk of peptide dose.

DETAILED DESCRIPTION OF THE INVENTION

The compositions and administration methods disclosed herein provide effective in vivo delivery of an oligonucleotide through dual molecular delivery of the oligonucleotide and a peptide containing conjugate. The oligonucleotide and the peptide containing conjugate are not covalently linked to each other and can be co-administered or sequentially administered to a subject.

The use of dual molecular delivery disclosed herein provides the unexpected benefits of effective in vivo cytosolic delivery of the oligonuleotide by directing the oligonucleotide to the site of action of a particular cell. The peptides may function as endosomolytic, cell penetrating and/or fusogenic agents. For example, the co-administered or sequentially administered peptide-containing conjugate helps with membrane translocation of the oligonucleotide and/or targeting of intended cells.

The oligonucleotide may be used directly as one component of the dual molecular delivery system. Alternatively, it can be attached to a targeting ligand, and optionally through a linker, to form a conjugate before administration. When present, the targeting ligands and/or linkers are attached to the oligonucleotide at different 2′-positions of the ribose rings and/or the terminal 3′ and/or 5′-positions of the oligonucleotide.

For peptide conjugates used herein, an optional linker may be present between each peptide and a targeting ligand. Multiple peptides and/or multiple linkers and ligands may be used in the conjugates.

In one embodiment, a method for inhibiting expression of a gene of a subject comprises administering:

(1) a composition comprising

to the subject; wherein:

R is an oligonucleotide with the ability to inhibit expression of a gene;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4;

X is a lipid;

P is a peptide selected from Table 2; and

each of a and b is independently 0, 1, 2, 3 or 4; and

(2) a composition comprising (P)_(c)-(L)_(d)-(G)_(e) to the subject; wherein:

P is a peptide and each occurance of P is independently selected from Table 2;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4;

d is 0, 1, 2, 3, 4, 5 or 6; and

each of c and e is independently 1, 2, 3, 4, 5 or 6.

In one embodiment, a method for inhibiting expression of a gene of a subject comprises administering:

(1) a composition comprising R-(L)_(a)-(G)_(b) to the subject; wherein:

R is an oligonucleotide with the ability to inhibit expression of a gene;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4; and

each of a and b is independently 0, 1, 2, 3 or 4; and

(2) a composition comprising (P)_(c)-(L)_(d)-(G)_(e) to the subject; wherein:

P is a peptide and each occurance of P is independently selected from Table 2;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4;

d is 0, 1, 2, 3, 4, 5 or 6; and

each of c and e is independently 1, 2, 3, 4, 5 or 6.

In one embodiment, a method for inhibiting expression of a gene of a subject comprises administering to the subject a composition comprising:

wherein:

R is an oligonucleotide with the ability to inhibit expression of a gene;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4;

X is a lipid;

P is a peptide selected from Table 2; and

each of a and b is independently 0, 1, 2, 3 or 4; and

(2) (P)_(c)-(L)_(d)-(G)_(e); wherein:

P is a peptide and each occurance of P is independently selected from Table 2;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4;

d is 0, 1, 2, 3, 4, 5 or 6; and

each of c and e is independently 1, 2, 3, 4, 5 or 6.

In one embodiment, a method for inhibiting expression of a gene of a subject comprises administering to the subject a composition comprising:

(1) R-(L)_(a)-(G)_(b); wherein:

R is an oligonucleotide selected from the group consisting of DNA, RNA, siRNA, and microRNA;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4; and

each of a and b is independently 0, 1, 2, 3 or 4; and

(2) (P)_(c)-(L)_(d)-(G)_(e); wherein:

P is a peptide and each occurance of P is independently selected from Table 2;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4;

d is 0, 1, 2, 3, 4, 5 or 6; and

each of c and e is independently 1, 2, 3, 4, 5 or 6.

In one embodiment of the above inhibition methods, R is an oligonucleotide selected from the group consisting of DNA, RNA, siRNA, and microRNA.

In one embodiment, a method for expressing a protein or polypeptide in a subject comprises administering:

(1) a composition comprising

to the subject; wherein:

R is an oligonucleotide with the ability to encode a protein or polypeptide;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4;

X is a lipid;

P is a peptide selected from Table 2; and

each of a and b is independently 0, 1, 2, 3 or 4; and

(2) a composition comprising (P)_(c)-(L)_(d)-(G)_(e) to the subject; wherein:

P is a peptide and each occurance of P is independently selected from Table 2;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4;

d is 0, 1, 2, 3, 4, 5 or 6; and

each of c and e is independently 1, 2, 3, 4, 5 or 6.

In one embodiment, a method for expressing a protein or polypeptide in a subject comprises administering:

(1) a composition comprising R-(L)_(a)-(G)_(b) to the subject; wherein:

R is an oligonucleotide with the ability to encode a protein or polypeptide;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4; and

each of a and b is independently 0, 1, 2, 3 or 4; and

(2) a composition comprising (P)_(c)-(L)_(d)-(G)_(e) to the subject; wherein:

P is a peptide and each occurance of P is independently selected from Table 2;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4;

d is 0, 1, 2, 3, 4, 5 or 6; and

each of c and e is independently 1, 2, 3, 4, 5 or 6.

In one embodiment, a method for expressing a protein or polypeptide in a subject comprises administering to the subject a composition comprising:

wherein:

R is an oligonucleotide with the ability to encode a protein or polypeptide;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4;

X is a lipid;

P is a peptide selected from Table 2; and

each of a and b is independently 0, 1, 2, 3 or 4; and

(2) (P)_(c)-(L)_(d)-(G)_(e); wherein:

P is a peptide and each occurance of P is independently selected from Table 2;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4;

d is 0, 1, 2, 3, 4, 5 or 6; and

each of c and e is independently 1, 2, 3, 4, 5 or 6.

In one embodiment, a method for expressing a protein or polypeptide in a subject comprises administering to the subject a composition comprising:

(1) R-(L)_(a)-(G)_(b); wherein:

R is an oligonucleotide with the ability to encode a protein or polypeptide;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4; and

each of a and b is independently 0, 1, 2, 3 or 4; and

(2) (P)_(c)-(L)_(d)-(G)_(c) to the subject; wherein:

P is a peptide and each occurance of P is independently selected from Table 2;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4;

d is 0, 1, 2, 3, 4, 5 or 6; and

each of c and e is independently 1, 2, 3, 4, 5 or 6.

In one embodiment of the above expression methods, R is an oligonucleotide selected from the group consisting of DNA, RNA, and mRNA.

In one embodiment of the above methods, R is a ds siRNA or ss siRNA.

In one embodiment of the above methods, occurance of P is independently selected from Table 2a.

In one embodiment of the above methods, occurance of P is independently selected from Table 2b.

In one embodiment of the above methods, each occurance of L is independently selected from Table 3a.

In one embodiment of the above methods, each occurance of G is independently selected from Table 4a.

In one embodiment of the above methods, G comprises:

wherein Ac is acetyl; wherein each X is independently —O—, —S—, —CH₂— or —NH—; each n is independently 1, 2, 3, or 4; and the bond with “

” indicates the point of attachment.

In one embodiment of the above methods, G comprises:

In one embodiment of the above methods, each of a and b is independently 0, 1 or 2; c is 1 or 2; and each of d and e is independently 1, 2 or 3.

In one embodiment of the above methods, each of a and b is independently 0 or 1; c is 1; and each of d and e is independently 1 or 2.

In one embodiment of the above methods, each of a and b is 1; c is 1; and each of d and e is 1.

In one embodiment, a method comprises:

(1) administering a composition comprising R-(L)_(a)-(G)_(b) to the subject; wherein:

R is an siRNA;

L is a linker and each occurance of L is independently selected from Table 3a;

G is a targeting ligand and each occurance of G is independently selected from Table 4a; and

each of a and b is independently 0, 1 or 2; and

(2) administering a composition comprising (P)_(c)-(L)_(d)-(G)_(e) to the subject; wherein:

P is a peptide and each occurance of P is independently selected from Table 2b;

L is a linker and each occurance of L is independently selected from Table 3a;

G is a targeting ligand and each occurance of G is independently selected from Table 4a; and

each of c, d and e is independently 1, 2 or 3.

In one embodiment of the above methods:

L of R-(L)_(a)-(G)_(b) is

G of R-(L)_(a)-(G)_(b) is:

each of a and b is 1; and

(P)_(c)-(L)_(d)-(G)_(e) of composition (2) is:

wherein P is a peptide selected from Table 2b; and

wherein L of composition (2) is selected from:

In one embodiment of the above methods, each L of compositions (1) and (2) is independently

In one embodiment of the above methods, R-(L)_(a)-(G)_(b) further comprises a lipid.

In one embodiment of the above methods, R-(L)_(a)-(G)_(b) further comprises a peptide.

In one embodiment of the above methods, (P)_(c)-(L)_(d)-(G)_(e) further comprises a lipid.

In one embodiment of the above methods, (P)_(c)-(L)_(d)-(G)_(e) further comprises an oligonucleotide.

In one embodiment of the above methods, the composition comprising R-(L)_(a)-(G)_(b) and the composition comprising (P)_(c)-(L)_(d)-(G)_(e) are co-administered at the same time. In one embodiment, the two compositions are in the same formulation. In another embodiment, the two compositions are in different formulations.

In one embodiment of the above methods, the composition comprising (P)_(c)-(L)_(d)-(G)_(e) and the composition comprising R-(L)_(a)-(G)_(b) are sequentially administered about 0.1 hour to 2 hours apart.

In one embodiment of the above methods, the composition comprising (P)_(c)-(L)_(d)-(G)_(e) and the composition comprising R-(L)_(a)-(G)_(b) are sequentially administered to a subject about 0.1 hour to 24 hours apart. In another embodiment the sequential administrations are about 0.1 hour to 6 hours apart. In another embodiment the sequential administrations are about 0.25 hour to 2 hours apart. In another embodiment the sequential administrations are about 0.25 hour to 1 hour apart. In another embodiment the sequential administrations are about 0.25 hour to 0.5 hour apart. In another embodiment the sequential administrations are about 0.25 hour apart.

In one embodiment of the above methods, the composition comprising (P)_(c)-(L)_(d)-(G)_(e) is administered about 0.1 hour to 2 hours before the composition comprising R-(L)_(a)-(G)_(b) is administered to a subject. In another embodiment, the composition comprising (P)_(c)-(L)_(d)-(G)_(e) is administered about 0.1 hour to 1 hour before the composition comprising R-(L)_(a)-(G)_(b) is administered to a subject. In another embodiment, the composition comprising (P)_(c)-(L)_(d)-(G)_(e) is administered about 0.25 hour to 0.5 hour before the composition comprising R-(L)_(a)-(G)_(b) is administered to a subject.

In one embodiment of the above methods, the composition comprising (P)_(c)-(L)_(d)-(G)_(e) is administered about 0.1 hour to 24 hours after the composition comprising R-(L)_(a)-(G)_(b) is administered to a subject. In another embodiment, the composition comprising (P)_(c)-(L)_(d)-(G)_(e) is administered about 0.1 hour to 12 hours after the composition comprising R-(L)_(a)-(G)_(b) is administered to a subject. In another embodiment, the composition comprising (P)_(c)-(L)_(d)-(G)_(e) is administered about 0.25 hour to 6 hours after the composition comprising R-(L)_(a)-(G)_(b) is administered to a subject. In another embodiment, the composition comprising (P)_(c)-(L)_(d)-(G)_(e) is administered about 0.25 hour to 2 hours after the composition comprising R-(L)_(a)-(G)_(b) is administered to a subject. In another embodiment, the composition comprising (P)_(c)-(L)_(d)-(G)_(e) is administered about 0.25 hour to 1 hour after the composition comprising R-(L)_(a)-(G)_(b) is administered to a subject. In another embodiment, the composition comprising (P)_(c)-(L)_(d)-(G)_(e) is administered about 0.25 hour to 0.5 hour after the composition comprising R-(L)_(a)-(G)_(b) is administered to a subject.

In one embodiment of the above methods, the compositions of oligonucleotide and peptide are dosed either by intravenous (i.v.) or subcutaneous (s.c.) injections. In another embodiment, the compositions are dosed by intravenous (i.v.) injections. In another embodiment, the compositions are dosed by subcutaneous (s.c.) injections.

In one embodiment of the above methods, the oligonucleotide composition is administered at a dose of 0.1 to 20 mg/kg (mpk). In another embodiment, the oligonucleotide composition is administered at a dose of 0.1 to 10 mpk. In another embodiment, the oligonucleotide composition is administered at a dose of 0.1 to 5 mpk. In another embodiment, the oligonucleotide composition is administered at a dose of 0.1 to 2 mpk. In another embodiment, the oligonucleotide composition is administered at a dose of 0.1 to 1 mpk. In another embodiment, the oligonucleotide composition is administered at a dose of 0.5 mpk.

In one embodiment of the above methods, the peptide composition is administered at a dose of 0.1 to 500 mpk. In another embodiment, the peptide composition is administered at a dose of 1 to 200 mpk. In another embodiment, the peptide composition is administered at a dose of 1 to 100 mpk. In another embodiment, the peptide composition is administered at a dose of 5 to 60 mpk. In another embodiment, the peptide composition is administered at a dose of 10 to 50 mpk.

In one embodiment of the above methods, the oligonucleotide composition is administered at a dose of 0.1 to 5 mpk; and the peptide composition is administered at a dose of 1 to 100 mpk

In one embodiment, a composition for dual molecular delivery of an oligonucleotide and a peptide conjugate comprises:

(1) R-(L)_(a)-(G)_(b); and

(2) (P)_(c)-(L)_(d)-(G)_(e); wherein:

R is an oligonucleotide selected from the group consisting of DNA, RNA, siRNA, and microRNA;

P is a peptide and each occurance of P is independently selected from Table 2;

L is a linker and each occurance of L is independently selected from Table 3;

G is a targeting ligand and each occurance of G is independently selected from Table 4;

each of a and b is independently 0, 1, 2, 3 or 4; and

each of c, d and e is independently 1, 2, 3, 4, 5 or 6.

In one embodiment of the above composition, each occurance of P is independently selected from Table 2a.

In one embodiment of the above composition, each occurance of P is independently selected from Table 2b.

In one embodiment of the above composition, each occurance of L is independently selected from Table 3a.

In one embodiment of the above composition, each occurance of G is independently selected from Table 4a.

In one embodiment of the above composition, each of a and b is independently 0, 1 or 2. In another embodiment, each of a and b is 0. In another embodiment, each of a and b is 1.

In one embodiment of the above composition, each of c, d and e is independently 1, 2 or 3. In another embodiment, each of c, d and e is 1.

In one embodiment of the above composition:

R is an siRNA;

each occurance of P is independently selected from Table 2b;

each occurance of L is independently selected from Table 3a;

each occurance of G is independently selected from Table 4a;

each of a and b is independently 0, 1 or 2;

c is 1 or 2; and

each of d and e is independently 1, 2 or 3.

In one embodiment of the above composition, G comprises a ligand of the following formula:

wherein each X is independently —O—, —S—, —CH₂— or —NH—; each n is independently 1, 2, 3, or 4; and the bond with “

” indicates the point of attachment.

In another embodiment, G of the above composition comprises a ligand of the following formula:

In one embodiment of the above composition, each of a and b is independently 0 or 1; c is 1; and each of d and e is 1.

In one embodiment of the above composition:

(1) G of R-(L)_(a)-(G)_(b) is:

each of a and b is 1; and

(2) (P)_(c)-(L)_(d)-(G)_(e) is:

wherein P is a peptide selected from Table 2b; and

wherein each L of compositions (1) and (2) is independently selected from:

In one embodiment of the oligonucleotide composition, the oligonucleotide is a double stranded siRNA; and G is attached to the guide and/or passenger strand of the siRNA, wherein the point of attachment is at a 2′-position of a ribose ring and/or at a terminal 3′ and/or 5′-position.

In one embodiment, the composition of R-(L)_(a)-(G)_(b) further comprises a lipid or solubilizing agent.

In one embodiment, the composition of R-(L)_(a)-(G)_(b) further comprises a lipid.

In one embodiment, the composition of R-(L)_(a)-(G)_(b) further comprises a peptide.

In one embodiment, the composition of (P)_(c)-(L)_(d)-(G)_(e) further comprises a lipid.

In one embodiment, the composition of (P)_(c)-(L)_(d)-(G)_(e) further comprises an oligonucleotide.

In one embodiment, disclosed herein is a method for inhibiting the expression of one or more genes. The method comprises contacting one or more cells with a therapeutically effective amount of an oligonucleotide composition of the invention together with a peptide containing conjugate, wherein the effective amount is an amount that suppresses the expression of the one or more genes. The method can be performed in vitro, ex vivo or in vivo.

In one embodiment, disclosed herein is a method for expressing a protein or polypeptide of a gene. The method comprises contacting one or more cells with a therapeutically effective amount of an oligonucleotide composition of the invention together with a peptide containing conjugate, wherein the effective amount is an amount that suppresses the expression of the one or more genes. The method can be performed in vitro, ex vivo or in vivo.

The methods and compositions of the invention can be used for the treatment of any disease or disorder known in the art, and for the treatment of any subject, e.g., any animal, any mammal, such as any human. One of ordinary skill in the art will also recognize that the methods and compositions of the invention may be used for the treatment of any disease that would benefit from downregulating or silencing a gene or genes.

The methods and compositions of the invention may be used with any dosage and/or formulation described herein, or any dosage or formulation known in the art. In addition to the routes of administration described herein, a person skilled in the art will also appreciate that other routes of administration may be used to administer the modular composition of the invention.

Oligonucleotide

An “oligonucleotide” as used herein, is a double stranded or single stranded, unmodified or modified RNA or DNA, including mRNA. Examples of modified RNAs include those which have greater resistance to nuclease degradation than do unmodified RNAs. Further examples include those which have a 2′ sugar modification, a base modification, a modification in a single strand overhang, for example a 3′ single strand overhang, or, particularly if single stranded, a 5′ modification which includes one or more phosphate groups or one or more analogs of a phosphate group. Examples and a further description of oligonucleotides can be found in WO2009/126933, which is hereby incorporated by reference.

In an embodiment, an oligonucleotide is an antisense, miRNA or siRNA. In one embodiment, the siRNA is a double stranded siRNA (ds siRNA). In another embodiment, the siRNA is a single stranded siRNA (ss siRNA). In an embodiment, the oligonucleotide is the passenger strand of an siRNA. In an embodiment, the oligonucleotide is the guide strand of an siRNA. In an embodiment, an oligonucleotide is mRNA.

siRNA

siRNA directs the sequence-specific silencing of mRNA through a process known as RNA interference (RNAi). The process occurs in a wide variety of organisms, including mammals and other vertebrates. Methods for preparing and administering siRNA and their use for specifically inactivating gene function are known. siRNA includes modified and unmodified siRNA. Examples and a further description of siRNA can be found in WO2009/126933, which is hereby incorporated by reference.

A number of exemplary routes of delivery as described in the Example section can be used to administer siRNA to a subject. In addition, the siRNA can be formulated according to any exemplary method known in the art. Examples and a further description of siRNA formulation and administration can be found in WO2009/126933, which is hereby incorporated by reference.

In some embodiments, siRNA sequences shown in Table 1 as well as their unmodified equivalents are suitable for compositions and methods as described herein and used in the Example section.

TABLE 1 Sequence Gene SEQ ID Code Target Strand Sequence NO siRNA-I CTNNB1 passenger [6 amiL][iB][omeC][omeU][fluG]omeU][omeU][fluG][fluG][fluA] 1803 [omeU][omeU][fluG][fluA][omeU][omeU][omeC][fluG][fluA][fluA] [fluA][omeUs][omeU][iB] CTNNB1 guide [omeUs][fluUs][omeUs][fluC][omeG][fluA][omeA][fluU][omeC] 1804 [fluA][omeA][fluU][omeC][fluC][omeA][fluA][omeC][fluA][omeG] [omeUs][omeU] siRNA-II CTNNB1 passenger [6amiL][iB][omeC][omeU][fluG][omeU][omeU][fluG][fluG][fluA] 1803 [omeU][omeU][fluG][fluA][omeU][omeU][omeC][fluG][fluA] [fluA][omeUs][omeU][iB] CTNNB1 guide [vinylP3dTs][fluU]omeU][fluC][omeG][fluA][omeA][fluU][omeC] 1805 [fluA][omeA][fluU][omeC][fluC][omeA][fluA][omeC][fluA][omeG] [omeUs][omeU] siRNA-III CTNNB1 passenger [6amiL][iB][omeC][omeU][fluG][omeU][omeU][fluG][fluG][fluA] 1803 [omeU][omeU][fluG][fluA][omeU][omeU][omeC][fluG][fluA][fluA] [fluA][omeUs][omeU][iB] CTNNB1 guide [vinylPmoeT][fluU][omeU][fluC][omeG][fluA][omeA][fluU][omeC] 1806 [fluA][omeA][fluU][omeC][fluC][omeA][fluA][omeC][fluA][omeG] [omeUs][omeU] sIRNA-IV CTNNB1 passenger [6amiL][iB][omeC][omeU][fluG][omeU][omeU][fluG][fluG][fluA] 1807 [omeU][omeU][fluG][fluA][omeU][omeU][omeC][fluG][clickA] [fluA][fluA][omeUs][omeU][iB][5Chol] CTNNB1 guide [vinylPmoeT][fluU][omeU][fluC][omeG][fluA][omeA][fluU][omeC] 1806 [fluA][omeA][fluU][omeC][fluC][omeA][fluA][omeC][fluA][omeG] [omeUs][omeU] siRNA-V CTNNB1 passenger [6amiL][iB][omeC][omeU][fluG][omeU][omeU][fluG][fluG][fluA] 1803 [omeU][omeU][fluG][fluA][omeU][omeU][omeC][fluG][fluA][fluA] [fluA][omeUs][omeU][iB] CTNNB1 guide [omeU][fluU][omeU][fluC][omeG][fluA][omeA][fluU][omeC][fluA] 1808 [omeA][fluU][omeC][fluC][omeA][fluA][omeC][fluA][omeG] [omeUs][omeU] sIRNA-VI CTNNB1 passenger [6amiL][iB][omeC][omeU][fluG][omeU][omeU][fluG][fluG][fluA] 1803 [omeU][omeU][fluG][fluA][omeU][omeU][omeC][fluG][fluA][fluA] [fluA][omeUs][omeU][iB] CTNNB1 guide [fluU][fluU][fluU][omeC][fluG][fluA][fluA][omeU][omeC][fluA][fluA] 1809 [omeU][omeC][fluC][fluA][fluA][omeC][fluA][fluG][omeUs] [omeU] Note: As used herein, ome = 2′ methoxy; flu = 2′ fluoro; click = 2′ propagyl; iB = inverted abasic; ″s″ subscript = phosphorothioate; r = 2′ ribo; and 6amil = n-hexylamino. vinylPmoeT

vinylP3dTs

Peptides

For macromolecular drugs and hydrophilic drug molecules, which cannot easily cross bilayer membranes, entrapment in endosomal/lysosomal compartments of the cell is thought to be the biggest hurdle for effective delivery to their site of action. Without wishing to be bound by theory, it is believed that the use of peptides will facilitate oligonucleotide escape from these endosomal/lysosomal compartments or oligonucleotide translocation across a cellular membrane and release into the cytosolic compartment. In certain embodiments, the peptides of the present invention may be polycationic or amphiphilic or polyanionic peptides or peptidomimetics which show pH-dependent membrane activity and/or fusogenicity. A peptidomimetic may be a small protein-like chain designed to mimic a peptide.

In some embodiments, the peptide is a cell-permeation agent, preferably a helical cell-permeation agent. These peptides are commonly referred to as Cell Penetrating Peptides. See, for example, “Handbook of Cell Penetrating Peptides” Ed. Langel, U.; 2007, CRC Press, Boca Raton, Fla. Preferably, the component is amphipathic. The helical agent is preferably an alpha-helical agent, which preferably has a lipophilic and a lipophobic phase. A cell-permeation agent can be, for example, a cell permeation peptide, cationic peptide, amphipathic peptide or hydrophobic peptide, e.g. consisting primarily of Tyr, Trp and Phe, dendrimer peptide, constrained peptide or crosslinked peptide. Examples of cell penetrating peptides include Tat, Penetratin, and MPG. For the present invention, it is believed that the cell penetrating peptides can be a “delivery” peptide, which can carry large polar molecules including peptides, oligonucleotides, and proteins across cell membranes. Cell permeation peptides can be linear or cyclic, and include D-amino acids, “retro-inverso” sequences, nonpeptide or pseudo-peptide linkages, peptidyl mimics. In addition the peptide and peptide mimics can be modified, e.g. glycosylated, pegylated, or methylated. Examples and a further discription of peptides can be found in WO2009/126933, which is hereby incorporated by reference. Synthesis of peptides is well known in the art.

The peptides may be conjugated through either end or both ends by addition of a cysteine or other thiol containing moiety to the C- or N-terminus. When not functionalized on the N-terminus, peptides may be capped by an acetyl group, or may be capped with a lipid, a PEG, or a targeting moiety. When the C-terminus of the peptides is unconjugated or unfunctionalized, it may be capped as an amide, or may be capped with a lipid, a PEG, or a targeting moiety.

Suitable peptides that can be used in the conjugates disclosed herein are listed in Table 2.

TABLE 2 Suitable Peptide Sequences Peptide SEQUENCE SEQ ID No. CGLFEAIEEFIENLWELLIDGWYGYGRKKRRQRR SEQ ID NO: 1 CGLFEAIEGFIENGWEGMIDGWYGYGHKKHHQHH SEQ ID NO: 2 C-bAla-LFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 3 CGLFEAIEGFIENGLKGLIDWWYGYGRKKRRQRR SEQ ID NO: 4 CGLFEAIEGFIEWGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 5 CRRQRRKKRGYGYWGDIMGEWGNEIFGEIAEFLG SEQ ID NO: 6 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQR SEQ ID NO: 7 CYGRKKRRQRRGLFEAIEGFIENGWEGMIDGWYG SEQ ID NO: 8 CIFGAIAGFIKNILKGLIDG SEQ ID NO: 9 CIFGAIAGFIRNIW SEQ ID NO: 10 CGLFHALLHLLHSLWHGLLHAWYGYGHKKHHQHR SEQ ID NO: 11 CGLFEAIEGLIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 12 CGLFELIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 13 CGLFEAIEGFIENGWEGLIDGWYGYGOOOOOQRR (O = ornithine) SEQ ID NO: 14 CGLFGAIEGFIENGWEGLIDGWYGYGRKKRRQRR SEQ ID NO: 15 CGLFEAIEGFLENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 16 CGLFEAIEGFIENGLEGMIDGWYGYGRKKRRQRR SEQ ID NO: 17 CGLFGAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 18 CGLFEAIEGFIENGWEG-Nle-IDGWYGYGRKKRRQRR SEQ ID NO: 19 CGIFGAIAGFIKNIWKGLIDW SEQ ID NO: 20 CYGRKKRRQRRGLFEAIEGFIENGWKGLIDAWYG SEQ ID NO: 21 CGLLEALEGLLESLWEGLLEAWYGYGRKKRRQRR SEQ ID NO: 22 CGLFEAIEGFIENGWEGMIDNWYGYGRKKRRQRR SEQ ID NO: 23 CIFGAIAGFIKNIWEGLIEAWYGLHLLHHLLHHLHHLLHHLLHL SEQ ID NO: 24 CIFGAIAGFIKNIWEGLIDAF SEQ ID NO: 25 CIFGAIAGFIKNIWEGLI SEQ ID NO: 26 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRRK(stearyl) SEQ ID NO: 27 CGLFEAIAGFIEGGWPGLINGWYGYGRKKRRQRRLHLLHHLLHHLHHLL SEQ ID NO: 28 HHLLHLLHHLLHHL CGLFEAIEGFIENGWEGMIDGWYGGGGLHLLHHLLHHLHHLLHHLLHLLH SEQ ID NO: 29 HLLHHL CGLFEAIEGFIENGWEGMIDGWYGLHLLHHLLHHLHHLLHHLLHL SEQ ID NO: 30 CGLFEALLELLESLWELLLEAYGRKKRRQRR SEQ ID NO: 31 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 32 CGLFEAIEGFIENGWEGMADGWYGYGRKKRRQRR SEQ ID NO: 33 CGIFGAIAGFIKNIWEGLIDWWYGYGRKKRRQRR SEQ ID NO: 34 CGFLPAIAGILSQLFEGLIDGWYGYGRKKRRQRR SEQ ID NO: 35 CFFGAIWGFIKSIL SEQ ID NO: 36 CIFGAIAGFIKNIWKGLIDWWYG SEQ ID NO: 37 CGLFEAIEGFIWNGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 38 CGLFEAIAEFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 39 CYGRKKRRQRRGLFEAIEGFIENGWKGLIDWWYG SEQ ID NO: 40 CGLFEAIEGFIEEGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 41 CGLFEAIEGFIENAWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 42 CGLFEAIEGFIENGWEGMIDLWYGYGRKKRRQRR SEQ ID NO: 43 CRLLRLLLRLWRRLLRLLR SEQ ID NO: 44 CGGFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 45 CGLFEKIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 46 CGLFEAIEGFIENGWENMIDGWYGYGRKKRRQRR SEQ ID NO: 47 CIFGAIAGFIKNILKGL SEQ ID NO: 48 CIFGAIAGFIKNILKGLIDGWYG SEQ ID NO: 49 CGLFEAIEGFIENGWEGMIDGWYG-(PEG)3-YGRKKRRQRR SEQ ID NO: 50 CGLFEALLELLESLWELLLEAYGRKKRRQRRLHLLHHLLHHLHHLLHHLL SEQ ID NO: 51 HL CYGRKKRRQRRWEAALAEALAEALAEHLAEALAEALEALAA SEQ ID NO: 52 CIFGAIAGFIKNIWEGLIDGWYGKLALKLALKALKAALKLA SEQ ID NO: 53 CFFGAIWEFIRSILEGLIDGWYGYGRKKRRQRR SEQ ID NO: 54 CGLFHALLHLLHSLWHLLLHAWYGYGRKKRRQRR SEQ ID NO: 55 CGLFHALLHLLHSLWHLLLHAWYGYGHKKHHQHR SEQ ID NO: 56 CGLFGALLELLESLWKGLLEWYGRKKRRQRR SEQ ID NO: 57 CRRQRRKKRGYGYWGDILGEWGNEIFGEIAEFLG SEQ ID NO: 58 CGLFEALEGFLENGWEGLLDGWYGYGROORRQRR (O = ornithine) SEQ ID NO: 59 CGLFGEIEELIENGLKNLIDWWYGYGRKKRRQRR SEQ ID NO: 60 CRRQRRKKRGYGYWWDILGKWGNEIFGEIAEFLG all (D) aminos SEQ ID NO: 61 CGIFGAIAGFIKNIL SEQ ID NO: 62 CGIFGAIAGLLKNIFK SEQ ID NO: 63 CIFGAIAGFIKNIWKGLIDW SEQ ID NO: 64 CIFGAIAGFIKNIWK SEQ ID NO: 65 CGLFEEIEGFIENGWEGLIDWWYGYGHKKHHQHR SEQ ID NO: 66 CGLFGEIEELIENGLKNLIDWWYGYGHKKHHQHR SEQ ID NO: 67 CGLFEEIEEFIENGWEGLIDWWYGYGHKKHHQHR SEQ ID NO: 68 stearyl-WEAALAEALAEALAEHLAEALAEALEALAAYGRKKRRQRRC SEQ ID NO: 69 CGLFEAIEGFIENGWKGLIDGWYGGLFEAIEGFIENGWKGLIDWWYG SEQ ID NO: 70 CGFFHAFFHFFHSFWHGFFEA SEQ ID NO: 71 CGNFGEIEELIEEGLENLIDWWNG SEQ ID NO: 72 CFFGAIWEFIRNILEGF SEQ ID NO: 73 CFFGAIWEFIHSIL SEQ ID NO: 74 CGLFHALLHLLHSLWHGLLEA SEQ ID NO: 75 CIFGAIAGFIKNIWEGL SEQ ID NO: 76 CIFGAIAGLLKNIFEGLIDGWYGYGRKKRRQRR SEQ ID NO: 77 CGFIGAIANLLSKIFEGLIDGWYGYGRKKRRQRR SEQ ID NO: 78 CGLFEAIEELIENLWKGLIDAWYGYGRKKRRQRR SEQ ID NO: 79 CGIFGAIAGLLKNIFKGLIDA SEQ ID NO: 80 CGIFGAIAGLLKNIFKGLIDW SEQ ID NO: 81 CGIFEAIAGLLKNIFK SEQ ID NO: 82 CGIFEEIAGLLKNIFK SEQ ID NO: 83 CGLFEAIAGFIEGGWPGLINGWYGYGRKKRRQRRLHLLHHLLHHLHHLL SEQ ID NO: 84 HHLLHL CGLFEAIEGFIENGWKGMIDWWYGYGRKKRRQRRK(stearyl) SEQ ID NO: 85 CGLFGEIEEFIENGWKGLIDWWYG SEQ ID NO: 86 CIFGAIAGFIKNIWLHLLHHLLHHLHHLLHHLLHL SEQ ID NO: 87 CGIFGAIEGFIENGWKGLIDAWYGYRKKRRQRR SEQ ID NO: 88 CELFGAIEGFIENGWKGLIDWWYGYGRKKRRQRR SEQ ID NO: 89 CIFGIDDLIIGLLFVAIVEAGIGGYLLGSYGRKKRRQRR SEQ ID NO: 90 GLFGALAEALAEALAEHLAEALAEALEALAAGGSC SEQ ID NO: 91 CGFIGAIANLLSKIFEGLIDGWYGYGRKKRRQRR all (D) SEQ ID NO: 92 CFFGAIWEFIRSILKGLI SEQ ID NO: 93 CFFGAIWEFIRSILK SEQ ID NO: 94 CFFGAIWEFIRSILE SEQ ID NO: 95 CIFGAIAGFIKNIWE SEQ ID NO: 96 CIFGAIAGFIKNIWKGLIDA SEQ ID NO: 97 CFFEAIEEFIKNILK SEQ ID NO: 98 CIFGAIAGLLRNIF SEQ ID NO: 99 CGIFGAIAGLLKNIW SEQ ID NO: 100 CLFGAIWEFIKSIL SEQ ID NO: 101 CFWGAIWEFIKSIL SEQ ID NO: 102 CFGGAIWEFIKSIL SEQ ID NO: 103 CFAGAIWEFIKSIL SEQ ID NO: 104 CGLFEAIEGFIENGWEGM(SO2)IDGWYGYGRKKRRQRR SEQ ID NO: 105 CGLFEAIEGFIENGWEGMIDWWYGYGRKKRRQRR SEQ ID NO: 106 CFFGAIWEFIKSIG SEQ ID NO: 107 CFFGAIWEFIKSIA SEQ ID NO: 108 CFFGAIWEFIKSIN SEQ ID NO: 109 CFFGAIWEFIKSIW SEQ ID NO: 110 CFFGAIWEFIKSILEGLIDWWYGYGHKKHHQHR SEQ ID NO: 111 Ac-CLHLLHHLLHHLHHLLHHLLHLLHHLLHHL SEQ ID NO: 112 Ac-LHLLHHLLHHLHHLLHHLLHLLHHLLHHLGGGRKKRRQRRRPPQC SEQ ID NO: 113 CRKKRRQRRRPPQGGGLHLLHHLLHHLHHLLHHLLHLLHHLLHHL SEQ ID NO: 114 CLHLLHHLLHHLHHLLHHLLHLLHHLLHHLGGGRKKRRQRRRPPQ SEQ ID NO: 115 CGLFHAIAHFIHGGWHGLIHGWYGYGRKKRRQRR SEQ ID NO: 116 CGLFKAIAKFIKGGWKGLIKGWYGYGRKKRRQRR SEQ ID NO: 117 CGLFEAIAGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 118 CWEAALAEALAEALAEHLAEALAEALEALAAYGRKKRRQRR SEQ ID NO: 119 CGLFEAIEGFIENGWEGMIDGWYGRKKRRQRRRPPQ SEQ ID NO: 120 GLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRRC SEQ ID NO: 121 Ac-LHLLHHLLHHLHHLLHHLLHLLHHLLHHLRKKRRQRRRPPQ SEQ ID NO: 122 Ac-LHLLHHLLHHLHHLLHHLLHLLHHLLHHLGPGRKKRRQRRRPPQ SEQ ID NO: 123 Ac-LIRLWSHLIHIWFQNRRLKWKKK SEQ ID NO: 124 Ac-RKKRRQRRRPPQQQQQQ SEQ ID NO: 125 Ac-GLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 126 Ac-LHLLHHLLHHLHHLLHHLLHLLHHLLHHLGGGRRRRRRRRR SEQ ID NO: 127 Ac-LHLLHHLLHHLHHLLHHLLHLLHHLLHHL-(Peg)12-RKKRRQRRRPPQ SEQ ID NO: 128 Ac-GLFGAIAGFIENGWEGMIDGWYGLIRLWSHLIWFQNRRLKWLLL SEQ ID NO: 129 Ac- SEQ ID NO: 130 HHHHHRKKRRQRRRPPQGGGLHLLHHLLHHLHHLLHHLLHLLHHLLHHL Ac-LHLLHHLLHHLHHLLHHLLHLLHHLLHHL-(Peg)2-RKKRRQRRRPPQ SEQ ID NO: 131 Ac- SEQ ID NO: 132 LHLLHHLLHHLHHLLHHLLLLHHLLHHLGGGRQIKIWFQNRRMKWKKGG Ac-KLLKLLLKLWLKLLKLLLKLLGGGRKKRRQRRRPPQ SEQ ID NO: 133 Ac-LHHLLHHLLHLLHHLLHHLHHLLHHLLHLC all (D) SEQ ID NO: 134 Ac-LHLLHHLLHHLHHLLHHLLHLLHHLLHHL-(PEG)6-RKKRRQRRRPPQC SEQ ID NO: 135 Ac-GLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRRC SEQ ID NO: 136 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR all (D) SEQ ID NO: 137 CGLFEAIEGFIENGWEGMIDGWYGYGRRRRRRRRR SEQ ID NO: 138 YGRKKRRQRRGLFEAIEGFIENGWEGMIDGWYGC SEQ ID NO: 139 CGVFVLGFLGFLATAGSYGRKKRRQRR SEQ ID NO: 140 CGLFKAIAKFIKGGWKGLIKGWYG SEQ ID NO: 141 CGLFEAIEGFIENGWEGMIDGWYGYGRKKR SEQ ID NO: 142 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRRYGRKKRRQRR SEQ ID NO: 143 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRRYGRKKRRQRR SEQ ID NO: 144 CGLFEAIKGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 145 CGLFEAIHGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 146 CGLFEAIRGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 147 CGLFEAIDGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 148 CRLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 149 CGGGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 150 CGLFEAIEGFIENGWEGMIDGWYGGGGYGRKKRRQRR SEQ ID NO: 151 CGLFEAIEGFIENGWEGMIDGWYG-(PEG)11-YGRKKRRQRR SEQ ID NO: 152 CFLGFLLGVGSAIASGIAVSKVLHL SEQ ID NO: 153 CGVFVLGFLGFLATAGSAMGARSLTLSAYGRKKRRQRR SEQ ID NO: 154 Ac-GLWRALWRLLRSLWRLLWRA-mercaptoethylamide SEQ ID NO: 155 C-Nle-LFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 156 CELFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 157 CGFFGAIAGFLEGGWEGMIAGWHGYGRKKRRQRR SEQ ID NO: 158 CFLGFLLGVGSAIASGIAVSKVLHLYGRKKRRQRR SEQ ID NO: 159 GLFEAIEGFIENGWEGLAEALAEALEALAAGGSC SEQ ID NO: 160 CGLFEAIEGFIENGWEGMIDGWYGLHLLHHLLHHLHHLLHHLLHLLHHLL SEQ ID NO: 161 HHL CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRRLHLLHHLLHHLHHLL SEQ ID NO: 162 HHLLHLLHHLLHHL CGLFGAIAGFIEGGWTGMIDGWYGYGRKKRRQRR SEQ ID NO: 163 CGLFGAIAGFIEGGWQGMVDGWYGYGRKKRRQRR SEQ ID NO: 164 CGLFGAIAGFIENGWQGLIDGWYGYGRKKRRQRR SEQ ID NO: 165 CGLFGAIAGFIENGWEGLVDGWYGYGRKKRRQRR SEQ ID NO: 166 CGLFGAIAGFIEGGWSGMIDGWYGYGRKKRRQRR SEQ ID NO: 167 CGLFGAIAGFIEGGWPGLVAGWYGYGRKKRRQRR SEQ ID NO: 168 CGLFGAIAGFIENGWEGMVDGWYGYGRKKRRQRR SEQ ID NO: 169 CGLFGAIAGFIEGGWPGLINGWYGYGRKKRRQRR SEQ ID NO: 170 CGLFGAIAGFIENGWEGLIDGWYGYGRKKRRQRR SEQ ID NO: 171 CGLFGAIAGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 172 CGLFGAIAGFIENGWEGMIDGWYGSSKKKK SEQ ID NO: 173 CGLFGAIAGFIENGWEGLIDGWYGYGRKKRRQRR SEQ ID NO: 174 CGLFEAIEGFIENGWEGLIDGWYGYGRKKRRQRR SEQ ID NO: 175 CGLFGAIAGFIENGWEGLIEGWYGGGRKKRRQRR SEQ ID NO: 176 CGLFEAIEGFIENGWEGMIDGWYGGGRKKRRQRR SEQ ID NO: 177 CGLFEAIAGFIENGWEGLIDGWYGYGRKKRRQRR SEQ ID NO: 178 CGLFEAIAEFIENGWEGLIEGWYGGRKKRRQRR SEQ ID NO: 179 CGLFEAIEGFIENGWEGMIDGWYGRKKRRQRRR SEQ ID NO: 180 CKLLKLLLKLWLKLLKLLLKLL SEQ ID NO: 181 CKLLKLLLKLWLKLLKLLLKLLYGRKKRRQRR SEQ ID NO: 182 GLFEAIEGFIENGWEGMIDGWYGC SEQ ID NO: 183 CVLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 184 CSLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 185 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQ SEQ ID NO: 186 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRR SEQ ID NO: 187 CGLFEAIEGFIENGWEGMIDGWYGYGKKKKKQKK SEQ ID NO: 188 CGLFEAIEGFIENGWEGMIDGWYGGLFEAIEGFIENGWEGMIDGWYG SEQ ID NO: 189 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRRGLFEAIEGFIENGWE SEQ ID NO: 190 GMIDGWYGYGRKKRRQRR RRQRRKKRGYGYWGDIMGEWGNEIFGEIAEFLGC SEQ ID NO: 191 CRRQRRKKRGYGYWGDIMGEWGNEIFGEIAEFLG SEQ ID NO: 192 GLFEAIEGFIENGWEGMIDGWYGYGRK-K(D)-RRQRR SEQ ID NO: 193 GLFEAIEGFIENGWEGMIDGWYGYGRKK-R(D)-RQRR SEQ ID NO: 194 GL-F(D)-EAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 195 GLF-E(D)-AIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 196 CGLFEAIEGFIENGWEGMIDGWYG SEQ ID NO: 197 CYGRKKRRQRR SEQ ID NO: 198 YGRKKRRQRRC SEQ ID NO: 199 RRQRRKKRGYGYWGDIMGEWGNEIFGEIAEFLGC all(D) SEQ ID NO: 200 CRRQRRKKRGYGYWGDIMGEWGNEIFGEIAEFLG all(D) SEQ ID NO: 201 CGLFEAIEGFIENGWEGMIDGAYGYGRKKRRQRR SEQ ID NO: 202 CGLFEALLELLESLWELLLEAWYGYGRKKRRQRR SEQ ID NO: 203 CGLFEAIEGFNENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 204 CGLFEAIEGFIENEWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 205 K(stearyl)GLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRRC SEQ ID NO: 206 CGLFEAIK(stearyl)GFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 207 CGLFEAIKGFIENGWEGMIDGWYGYGRK(stearoyl)KRRQRR SEQ ID NO: 208 CGLFEAIEGFIENPWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 209 (stearyl)GLFEAIEGFIENPWEGMIDGWYGYGRKKRRQRRC SEQ ID NO: 210 CGLFGAIAGFIEGGWPGLINGWYGYGRKKRRQRRLHLLHHLLHHLHHLL SEQ ID NO: 211 HHLLHLLHHLLHHL CGLFGAIAGFIEGGWPGLINGWYGYGRKKRRQRRLHLLHHLLHHLHHLL SEQ ID NO: 212 HHLLHL CGLFEAIAGFIEGGWPGLINGWYGYGRKKRRQRR SEQ ID NO: 213 CGLEEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 214 CGLFNAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 215 CGLFAAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 216 CGLFEAIENFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 217 CGLFEAIEKFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 218 CGLFEAIEGFAENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 219 CGLFEAIEGFIENWWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 220 CGLFEAIEGFIENNWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 221 CGLFEAIEGFIENGEEGMIDGWYGYGRKKRRQRR SEQ ID NO: 222 CGLFEAIEGFIENGWAGMIDGWYGYGRKKRRQRR SEQ ID NO: 223 CGLFEAIEGFIENGWNGMIDGWYGYGRKKRRQRR SEQ ID NO: 224 CGLFEAIEGFIENGWGGMIDGWYGYGRKKRRQRR SEQ ID NO: 225 CGLFEAIEGFIENGWEGMIDAWYGYGRKKRRQRR SEQ ID NO: 226 CGLFEAIEGFIENGWLGMIDGWYGYGRKKRRQRR SEQ ID NO: 227 CGLFEAIEGFIENGWKGMIDGWYGYGRKKRRQRR SEQ ID NO: 228 CGLFEAIEGFIENGWEGMIDKWYGYGRKKRRQRR SEQ ID NO: 229 CGLFEAIEGFIENGWEGMIDEWYGYGRKKRRQRR SEQ ID NO: 230 CGLFEAIEGFIENGWEGMIDGLYGYGRKKRRQRR SEQ ID NO: 231 CGLFEAIEGFIENGWEGMIDGNYGYGRKKRRQRR SEQ ID NO: 232 CGLFEAIEGFIENGWEGMIDGKYGYGRKKRRQRR SEQ ID NO: 233 CGLFEAIEGFIENGWEGMIDGEYGYGRKKRRQRR SEQ ID NO: 234 CGLFEALEELLEGGWEGLIEAWYGYGRKKRRQRR SEQ ID NO: 235 CELFGAIWEFIEGGWEGLIEAWYGYGRKKRRQRR SEQ ID NO: 236 CGLFEALEEFIEGGWEGLLEAWYGYGRKKRRQRR SEQ ID NO: 237 CGLFEALEEFIENGWEGLLEAWYGYGRKKRRQRR SEQ ID NO: 238 CGLFEAIEGFIESGWEGLIDGWYGYGRKKRRQRR SEQ ID NO: 239 CGLFEAIEEFIEGGWEGLIEAWYGYGRKKRRQRR SEQ ID NO: 240 CGLFEAIEGFIENGWEGLIDAWYGYGRKKRRQRR SEQ ID NO: 241 CGLFEAIEGFILNGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 242 CGLFEAIEGFIKNGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 243 CGLFEAIEGFIGNGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 244 CGLFEAIEGFIELGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 245 CGLFEAIEGFIEKGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 246 CGLFEAIAEFIEGGWEGLIEGWYGYGRKKRRQRR SEQ ID NO: 247 CRGWEVLKYWWNLLQY SEQ ID NO: 248 CRGWEVLKYWWNLLQYYGRKKRRQRR SEQ ID NO: 249 CGLFGAIAGFIENGWEGMIDGWYGFRYGRKKRRQRR SEQ ID NO: 250 Ac-CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR-CO2H SEQ ID NO: 251 CGLLEALEGLLENGWEGLLEAWYGYGRKKRRQRR SEQ ID NO: 252 CLRHLLRHLLRHLRHLLRHLRHLLRHLLRH SEQ ID NO: 253 CGIFEAIEGFIENGWEGIIDGWYGYGROORRQRR (O = ornithine) SEQ ID NO: 254 CGIGAVLKVLTTGLPALISWIKRKRQQ SEQ ID NO: 255 CGIGAVLKVLTTGLPALISWIHHHHQQ SEQ ID NO: 256 CGAFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 257 Ac-LHLLHHLLHHLHHLLHHLLHLLHHLLHHLRRRRR SEQ ID NO: 258 CGLFGAIWGFIENWWKGLIDWWYGYGRKKRRQRR SEQ ID NO: 259 CGLFGAIEGFIENGWKGLIDAWYGYGRKKRRQRR SEQ ID NO: 260 CGLFEAIAGFIENGWKGLIDWWYGYGRKKRRQRR SEQ ID NO: 261 GLFEAIEGFIENGWKGLIDWWYGYGRKKRRQRRC SEQ ID NO: 262 YGRKKRRQRRGLFEAIEGFIENGWKGLIDAWYGC SEQ ID NO: 263 YGRKKRRQRRGLFEAIEGFIENGWKGLIDWWYGC SEQ ID NO: 264 CGLFHAIHGFIENGWHGLIDWWYGYGRKKRRQRR SEQ ID NO: 265 CGLFEAIEGFIENGWKGLIDWWYGYGRKKRRQRRK(stearyl) SEQ ID NO: 266 CGLFKALLKLLKSLWKLLLKAWYGYGHKKHHQHR SEQ ID NO: 267 CGLFKALLKLLKSLWKGLLKAWYGYGHKKHHQHR SEQ ID NO: 268 CGLAKALLKLLKSLWKGLIEAWYGYGRKKRRQRR SEQ ID NO: 269 CGIFGAIAGFIKNIW SEQ ID NO: 270 CIFGAIAGFIKNIWEGLIDGWYGYGRKKRRQRR SEQ ID NO: 271 CGIFGAIAGFIKNIWEGLIDGYGRKKRRQRR SEQ ID NO: 272 CGIFGAIAGFIKNIWKGLIDAWYGYGRKKRRQRR SEQ ID NO: 273 CIFGAIAGFIKNIWKGLIDWWYGYGRKKRRQRR SEQ ID NO: 274 CLFGAIAGFIKNIW SEQ ID NO: 275 CGL(R5)EAIEGF(S8)ENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 276 CGLFEA(S5)EGF(S5)ENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 277 CGLFEAIEGFIENGWEGAIDGWYGYGRKKRRQRR SEQ ID NO: 278 CGLFEAIEGFIENGWEGEIDGWYGYGRKKRRQRR SEQ ID NO: 279 CGIFGAIAGFIKNGWEGMVDWYGYGRKKRRQRR SEQ ID NO: 280 CGLFEAIAGFIENGWEGMIDGWYGFYGRKKRRQRR SEQ ID NO: 281 CGIFGAIAGFIKNGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 282 CIFGAIAGFIKNIW SEQ ID NO: 283 CIFGAIAGFIKNIWYGRKKRRQRR SEQ ID NO: 284 CGIFGAIAGFIKNIWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 285 CGLFEAIEGFIENGWEGLIEAYGRKKRRQRR SEQ ID NO: 286 CGLFEALLGFIENGWEGLIDGYGRKKRRQRR SEQ ID NO: 287 CGLFGAIEGFIENGWEGLIDGWYGYGRKKRRQRRR SEQ ID NO: 288 CELFGAIEGFIENGWEGMIDGWYGYGRKKRRQRRR SEQ ID NO: 289 CGLFEAIEGFIENGWEGMIDGWYGYGHKKHHQHR SEQ ID NO: 290 CGLFGAIEGFIEGGWPGLINGWYGYGRKKRRQRRR SEQ ID NO: 291 CGLFKALLKLLKSLWKLLLKAYGRKKRRQRR SEQ ID NO: 292 CGLFKALLKLLKSLWKLLLKAWYGYGRKKRRQRR SEQ ID NO: 293 CGLFRALLRLLRSLWRLLLRAYGRKKRRQRR SEQ ID NO: 294 CGLFEAILGFIENGWEGLIDGWYGYGRKKRRQRR SEQ ID NO: 295 CGLFEAIWEFIENGWEGLIDGWYGYGRKKRRQRR SEQ ID NO: 296 CGLFEAIEGFIENGWEGMIDGWYGGGGLHLLHHLLHHLHHLLHHLLHL SEQ ID NO: 297 CGPVEDAITAAIGRVADTVGTYGRKKRRQRR SEQ ID NO: 298 CMDGTLFPGDDDLAIPATEFFSTKA SEQ ID NO: 299 CGLFEALEEFIEGGWEGLLEAWYGYGRKKRRQRR SEQ ID NO: 300 CGLFEALEEFIENGWEGLLEAWYGYGRKKRRQRR SEQ ID NO: 301 CELFGAIWEFIEGGWEGLIEAYGRKKRRQRR SEQ ID NO: 302 CGLFEAIEGFIEEGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 303 CGLFEAIAEFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 304 CGLFEAIAEFIEGLWEGLIEGWYGYGRKKRRQRR SEQ ID NO: 305 CGLLEALEGLLESLWEGLLEAWYGYGRKKRRQRR SEQ ID NO: 306 CGLFEAIEGFIENGWEGMIDIWYGYGRKKRRQRR SEQ ID NO: 307 CGLFEAIEGFIENGWRGMIDGWYGYGRKKRRQRR SEQ ID NO: 308 CGLFEAIEGFIENGWDGMIDGWYGYGRKKRRQRR SEQ ID NO: 309 CGLFEAIEGFIENHWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 310 CGLFEAIEGFIENWWKGLIDWWYGYGRKKRRQRR SEQ ID NO: 311 GLFEAIEGFIENGWKGLIDAWYGYGRKKRRQRRC SEQ ID NO: 312 CGLFEAIEGFIENGWKGMIDAWYGYGRKKRRQRR SEQ ID NO: 313 CGLFEAIEGFIENGWKGMIDWWYGYGRKKRRQRR SEQ ID NO: 314 CGLAEAIEGFIENGLKGLIDWWYGYGRKKRRQRR SEQ ID NO: 315 RRQRRKKRGYGYWGDILGEWGNEIFGEIAEFLGC all(D) SEQ ID NO: 316 CRRQRRKKRGYGYWGDILGEWGNEIFGEIAEFLG all(D) SEQ ID NO: 317 CGLFEAIEGFIENGWKGLIDWWYGYGRKKRRQRR SEQ ID NO: 318 CGFFEAIEGFIENGLKGLIDAWYGYGRKKRRQRR SEQ ID NO: 319 CGLFEAIEGFIENGLKGLIDAWYGYGRKKRRQRR SEQ ID NO: 320 CELFGAIEGFIENGWKGLIDAWYGYGRKKRRQRR SEQ ID NO: 321 CGLFKAIKGFIKNGWKGLIKAWYGYGRKKRRQRR SEQ ID NO: 322 CGLAEALLELLESLWKGLIEAYGRKKRRQRR SEQ ID NO: 323 CGIFGAIEGFIENGWKGLIDAWYGYGRKKRRQRR SEQ ID NO: 324 CGIAGAIAGFIKNIWEGLIDWWYGYGRKKRRQRR SEQ ID NO: 325 CGIAGAIAGFIKNIWKGLIDAWYGYGRKKRRQRR SEQ ID NO: 326 CGIFGAIAGFIKNIWEGLIDGWYGKKKKKKKKK SEQ ID NO: 327 CG(R5)FEAIEG(S8)IENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 328 CGLFEAIEGF(R5)ENGWEG(S8)IDGWYGYGRKKRRQRR SEQ ID NO: 329 GLFEAIEGFIENGWEGMIDGWYGCYGRKKRRQRR SEQ ID NO: 330 GLFEAIEGFIENGWEGMIDGWYGGCGYGRKKRRQRR SEQ ID NO: 331 GLLEALEGLLENGWEGLLDGWYGYGRKKRRQRR SEQ ID NO: 332 CFFGAIWEFIRNIL SEQ ID NO: 333 CIFGAIAGFIRSIL SEQ ID NO: 334 CGLFEEIEEFIENGWEGLIDWWYGYGRKKRRQRR SEQ ID NO: 335 CGFFGAIWEFIKSIL SEQ ID NO: 336 GFFGAIWEFIKSILC SEQ ID NO: 337 CGLFEALEGFIENGWEGLLDGWYGYGROORRQRR (O = ornithine) SEQ ID NO: 338 CGLFEALLELLENGWELLLEAWYGYGRKKRRQRR SEQ ID NO: 339 CGLFEALLELLENGWELLLDGWYGYGRKKRRQRR SEQ ID NO: 340 CALFEAIEAFIENGWEAMIDAWYGYGRKKRRQRR SEQ ID NO: 341 CGLFGAIWGFIENGWEGLIDGWYGYGRKKRRQRR SEQ ID NO: 342 CGLFEAIEELIENLWKGLIDWWYGYGRKKRRQRR SEQ ID NO: 343 CGLFEEIEGFIENGWKGLIDWWYGYGRKKRRQRR SEQ ID NO: 344 CGLFEEIEGFIENGWKGLIDWWYGYGHKKHHQHR SEQ ID NO: 345 CFFGAIWEFIKNILKGLIDGWYG SEQ ID NO: 346 CGIFGAIAGFIRSIL SEQ ID NO: 347 CGLFEEIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 348 CGLFEAIEGFIENGWEGMIDGWNGYGRKKRRQRR SEQ ID NO: 349 AGYLLGKINLKALAALAKKILHHHHHHKKKKKKC SEQ ID NO: 350 Bis CGLFEAIEGFIENGWEGMIDWWYGYGRKKRRQRR SEQ ID NO: 351 CGLFEAIEGFIENGWEGMIDGWYG-(PEG)6-YGRKKRRQRR SEQ ID NO: 352 CGIFGAIWNGIKSLFEGLIDGWYGYGRKKRRQRR SEQ ID NO: 353 CGIFGAIEGFIENGWEGLIDWWYGYGRKKRRQRR SEQ ID NO: 354 CIFGAIAGFIKNIWEGLIDWWYGYGRKKRRQRR SEQ ID NO: 355 CGLFEAIEGFIENGWKGLIDGWYGGLFEAIEGFIENGWKGLIDWWYG SEQ ID NO: 356 CWEAALAEALAEALAEHLAEALAEALEALAAYGRKKRRQRRK(stearyl) SEQ ID NO: 357 CGLFEAIEGFIENGWKGLIDWWYGYGRKKRRQRR SEQ ID NO: 358 CGLFEELEELLEEGWEGLLEAYGRKKRRQRR SEQ ID NO: 359 CGNFEEIEEFIEEGLRNFIDWWYGYGHKKHHQHR SEQ ID NO: 360 CFFGAIWEFIRNILEGLIDWWYGYGRKKRRQRR SEQ ID NO: 361 CFFGAIWEFIKNILLHLLHHLLHHLHHLLHHLLHL SEQ ID NO: 362 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR all(D) SEQ ID NO: 363 CGFFHAFFHFFHSFWHGFFEA SEQ ID NO: 364 CGLFHALLHLLHSLWHGLLHWWYGYGHKKHHQHR SEQ ID NO: 365 CGLFGALLELLESLWEGLLEWYGRKKRRQRR SEQ ID NO: 366 CGLFGALLELLESLWEGLLEWYGHKKHHQHR SEQ ID NO: 367 CGLFHALLHLLHSLWKGLLEWWYGF SEQ ID NO: 368 CIFGAIAGFIRSILEGF SEQ ID NO: 369 CGIFGAIAGFIKNIWKGLIDA SEQ ID NO: 370 CFFEAIEEFIKNIWK SEQ ID NO: 371 CGLFEAIEGFIENGWKGLIDWLAEALAEALEALAA SEQ ID NO: 372 GCGIFGAIAEFIKNIW SEQ ID NO: 373 CIFGAIAEFIKNIWKGLIDW SEQ ID NO: 374 CFFGAIWEFIKSILELLLEAYGHKKHHQHRR SEQ ID NO: 375 CWFGAIWEFIKSIL SEQ ID NO: 376 CAFGAIWEFIKSIL SEQ ID NO: 377 CFLGAIWEFIKSIL SEQ ID NO: 378 CFFGAIWEFIKSIK SEQ ID NO: 379 CGFIGAIANLLSKIFEGLIDGWYGYGRKKRRQRR all(D) SEQ ID NO: 380 CFFGAIWEFIKSIL SEQ ID NO: 381 CIFGAIAGFIKNIWLHLLHHLLHHLHHLLHHLLHL all(D) SEQ ID NO: 382 CFFGAIAEFIKNIW SEQ ID NO: 383 CIFEAIWGFIKNIW SEQ ID NO: 384 (stearyl)-AGYLLGKINLKALAALAKKILHHHHHHKKKKKKC SEQ ID NO: 385 CIFEAIAGFIKNIWKGLIDWWYGYGRKKRRQRR SEQ ID NO: 386 CGLFEAIEGFIENGWKGLIDWWYGGRPRESGKKRKRKRLKP SEQ ID NO: 387 C(b-Ala)GFGEIEEFIENGLKNLIDWWYGYGHKKHHQHR SEQ ID NO: 388 C(b-Ala)GFEFIEEFIENGLKNLIDWWYGYGRKKRRQRR SEQ ID NO: 389 C(b-Ala)GFEFIEEFIENGLKNLIDWWYGYGHKKHHQHR SEQ ID NO: 390 CGGIEEIAGLLSKILKGLIDWWYGYGHKKHHQHR SEQ ID NO: 391 CGFIGAIANLLSKIFEGLIDWWYGYGRKKRRQRR SEQ ID NO: 392 CGFIGAIAELLEKIFEGLIDWWYGYGRKKRRQRR SEQ ID NO: 393 CGFIGAIAELLEKIFEGLIDWWYGYGHKKHHQHR SEQ ID NO: 394 CFFGAIWEFIRNILEGLIDWWYGYGHKKHHQHR SEQ ID NO: 395 CFFGAIWEFIKSILLHLLHHLLHHLHHLLHHLLHL SEQ ID NO: 396 CFFGAIWEFIRSILLHLLHHLLHHLHHLLHHLLHL SEQ ID NO: 397 CGFFGAIWEFIRSILEGFIDWWYGYGYGHKKHHQHR SEQ ID NO: 398 CGLFEAIWEFIKSILEGLLEAYGHKKHHQHR SEQ ID NO: 399 CGLFEAIWEFIKSILEGLLEAWYGYGHKKHHQHR SEQ ID NO: 400 CGIFGAIAGFIKNIWKYGRKKRRQRR SEQ ID NO: 401 CGLFEALLELLESLWELLLEAWYGYGHKKHHQHR SEQ ID NO: 402 CIFGAIAGFIRNIWKGLIDGWYG SEQ ID NO: 403 CGIFGAIAGFIRNIWKGLIDGWYG SEQ ID NO: 404 CFFGAIWEFIKNILKLHLLHHLLHHLHHLLHHLLHL SEQ ID NO: 405 CFFGAIWEFIRNILLHLLHHLLHHLHHLLHHLLHL SEQ ID NO: 406 CFFGKIWEFIKSIL SEQ ID NO: 407 CYGRKKRRQRRGLFEALLELLESLWELLLEA SEQ ID NO: 408 FFGAIWEFIKSILC SEQ ID NO: 409 CWWGAIEGFIKSIL SEQ ID NO: 410 CFFGAIWEWIKSIL SEQ ID NO: 411 CFFGAIWEFWKSIL SEQ ID NO: 412 CFFGAIWEFIKFIL SEQ ID NO: 413 CFFGAIWEFIKKIL SEQ ID NO: 414 CFFGAIWEFIKGIL SEQ ID NO: 415 CFFGAIWEFIKLIL SEQ ID NO: 416 CFFGAIWEFIKWIL SEQ ID NO: 417 CFFGAIWEFIKSFL SEQ ID NO: 418 CFFGAIWEFIKSKL SEQ ID NO: 419 CFFGFIWEFIKSIL SEQ ID NO: 420 CIFGAIAGFIKNILKGLIDAF SEQ ID NO: 421 CFFGKIWELWEWIL SEQ ID NO: 422 CFFGAIWEFAKSIL SEQ ID NO: 423 CFFGAIWEFIKSAL SEQ ID NO: 424 CFFGAIWEFIKSWL SEQ ID NO: 425 CFFGAIWEFIKSILK SEQ ID NO: 426 CFFGAIWEFIKSILE SEQ ID NO: 427 CFFKAIWEFIKSIL SEQ ID NO: 428 CFFNAIWEFIKSIL SEQ ID NO: 429 CFFGGIWEFIKSIL SEQ ID NO: 430 CFFGNIWEFIKSIL SEQ ID NO: 431 CFFGALWEFIKSIL SEQ ID NO: 432 CFFGAAWEFIKSIL SEQ ID NO: 433 CGLFHALLHLLHSLWHGLLDG SEQ ID NO: 434 CGLFHALLHLLHSLWHGLLEW SEQ ID NO: 435 CGLFHALLHLLHSLWHLLLEA SEQ ID NO: 436 CGLFHALLHLLHSLWKLLLEW SEQ ID NO: 437 CKFGAIWEFIKSIL SEQ ID NO: 438 CFKGAIWEFIKSIL SEQ ID NO: 439 CFFGAIWKFIKSIL SEQ ID NO: 440 CFFGAIWAFIKSIL SEQ ID NO: 441 CFFGAIWLFIKSIL SEQ ID NO: 442 CFFGAIWFFIKSIL SEQ ID NO: 443 CFFGAIWNFIKSIL SEQ ID NO: 444 CFFGAIWELIKSIL SEQ ID NO: 445 CFFGAIWEAIKSIL SEQ ID NO: 446 CGLFEAIEGFIENGWEGLAEALAEALEALAAYGRKKRRQRR SEQ ID NO: 447 CIFGAIAGFIKNIWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 448 CIFGAIAGFIKNIWEGLIDAWYGYGRKKRRQRR SEQ ID NO: 449 CIFGAIAGFIKNIWKGLIDAWYGYGRKKRRQRR SEQ ID NO: 450 CIFGAIAGFIKNIWIFGAIAGFIKNIWWYGYGRKKRRQRR SEQ ID NO: 451 CGLFGAIAGFIENGWEGLIEGWYG SEQ ID NO: 452 CGLFEAIEGFIENGWEGLIDGWYGYGOOOOOQRR (O = ornithine) SEQ ID NO: 453 CGLFEAIEGFIENGWKGLIDWWYGYGRKKRRQRR SEQ ID NO: 454 CGLFEAIEGFIENGWEGLIDGWYGYGRKKRRQRRK(stearyl) SEQ ID NO: 455 CYGHKKHHQHRGLFEAIEGFIENGWKGLIDWWYG SEQ ID NO: 456 CYGHKKHHQHRGLFEAIEEFIENGWEGLIDGWYG SEQ ID NO: 457 CGLFEAIEGFIENGWKGLIDGWYGYGRKKRRQRRK(stearyl) SEQ ID NO: 458 CGLFEAIEGFIENGWHGMIDGWYGYGRKKRRQRR SEQ ID NO: 459 IFGIDDLIIGLLFVAIVEAGIGGYLLGSYGRKKRRQRRC SEQ ID NO: 460 CGFFGEIAELIEEGLKGLIDWWNG SEQ ID NO: 461 CGLFGEIEELIEEGLENLIDWWNG SEQ ID NO: 462 CFFGAIWEFIHSIL all (D) SEQ ID NO: 463 CFFGAIWEFIHNIL SEQ ID NO: 464 CFFGAIWEFIHSIFK SEQ ID NO: 465 CGIFEAIAGLLKWIFK SEQ ID NO: 466 CGIFELIAGLLKNIFK SEQ ID NO: 467 CGIFEAIAGLLKSILKK(stearyl) SEQ ID NO: 468 CGIFGAIAGLLKSILKK(stearyl) SEQ ID NO: 469 CIFGAIAGFIKNILKGL all (D) SEQ ID NO: 470 CIFGAIAGFIKNILKGLIDGWWYG SEQ ID NO: 471 CIFGAIAGFIKNIWHGLI SEQ ID NO: 472 CIFGAIAGFIKNILKGLK(stearyl) SEQ ID NO: 473 GLGKLINKIFGAIAGFIC all (D) SEQ ID NO: 474 CGIFEAIAGLLKNIFD SEQ ID NO: 475 CGIFEAIAGLLKNIFE SEQ ID NO: 476 CGIFEAIAGLLKNIFR SEQ ID NO: 477 CGIFEAIAGLLKNIFH SEQ ID NO: 478 CGIFEAIAGLLKNIFO (O = ORNITHINE) SEQ ID NO: 479 CGIFEAIAGLLKNIFN SEQ ID NO: 480 CGIFEAIAGLLKNIFCit (Cit = citrulline) SEQ ID NO: 481 CGIFEAIWGLLKNIFK SEQ ID NO: 482 CGIFGAIWGLLKNIFK SEQ ID NO: 483 CIFGAIAGLLKNIFK SEQ ID NO: 484 CIFEAIAGLLKNIFK SEQ ID NO: 485 CFFGAIAGLLKNIFK SEQ ID NO: 486 CFFEAIAGLLKNIFK SEQ ID NO: 487 CGFFEAIAGLLKNIFK SEQ ID NO: 488 CIFGAIAGFIKNIWEGLI all (D) SEQ ID NO: 489 CIFGAIAGLLKNIFK all(D) SEQ ID NO: 490 CGLFGEIEELIEEGLENLIDWWNG all(D) SEQ ID NO: 491 CGNFGEIEELIEEGLENLIDWWNG all(D) SEQ ID NO: 492 CGFFGEIAELIEEGLKGLIDWWNG all(D) SEQ ID NO: 493 CGLFGEIEELIEEGLENLIDWWNE SEQ ID NO: 494 CGFFGAIAGLLKNIFK SEQ ID NO: 495 CGLFELIEGFIENGWEGMIDGWYGYGRKKRRQRRK(stearyl) SEQ ID NO: 496 CGLFELIEGFIEWGWEGMIDGWYGYGRKKRRQRRK(stearyl) SEQ ID NO: 497 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRRK(2H,2H,3H,3H- SEQ ID NO: 498 perfluorononanoyl) CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRRK(2H,2H,3H,3H- SEQ ID NO: 499 perfluoro-10 methylundecanoyl) CIFGAIAGFIKNIWEGLIK(2H,2H,3H,3H-perfluorononanoyl) SEQ ID NO: 500 CIFGAIAGFIKNIWEGLIK(2H,2H,3H,3H-perfluoro-10 methylundecanoyl) SEQ ID NO: 501 CGLFEAIEGFIEWGWEGMIDGWYGYGRKKRRQRRK(2H,2H,3H,3H- SEQ ID NO: 502 perfluorononanoyl) CGLFEAIEGFIEWGWEGMIDGWYGYGRKKRRQRRK(2H,2H,3H,3H- SEQ ID NO: 503 perfluoro-10 methylundecanoyl) CGLFELIEGFIENGWEGMIDGWYGYGRKKRRQRRK(2H,2H,3H,3H- SEQ ID NO: 504 perfluorononanoyl) CGLFELIEGFIENGWEGMIDGWYGYGRKKRRQRRK(2H,2H,3H,3H- SEQ ID NO: 505 perfluoro-10 methylundecanoyl) CFFGAIWEFIHSILK(2H,2H,3H,3H-perfluorononanoyl) SEQ ID NO: 506 CFFGAIWEFIHSILK(2H,2H,3H,3H-perfluoro-10 methylundecanoyl) SEQ ID NO: 507 CIFGAIAGFIKNILKGLK(2H,2H,3H,3H-perfluorononanoyl) SEQ ID NO: 508 CIFGAIAGFIKNILKGLK(2H,2H,3H,3H-perfluoro-10 methylundecanoyl) SEQ ID NO: 509 CFFGAIWEFIRNILEGFK(2H,2H,3H,3H-perfluorononanoyl) SEQ ID NO: 510 CFFGAIWEFIRNILEGFK(2H,2H,3H,3H-perfluoro-10 methylundecanoyl) SEQ ID NO: 511 CGLFGEIEELIEEGLENLIDWWNQ SEQ ID NO: 512 CGIFGAIAGLLKSALK SEQ ID NO: 513 CGIFEAIAGLLKSIWK SEQ ID NO: 514 CGIFEAIAGLLKSILK SEQ ID NO: 515 CGIFEAIAGLLONIFK (O = Ornithine) SEQ ID NO: 516 CGIFEAIAGLLKNILKGLIDGWYG SEQ ID NO: 517 CGIFGAIAGLLKNILKGLIDGWYG SEQ ID NO: 518 CGIFGAIAGLLKNIFKGLIDGWYG SEQ ID NO: 519 CGIFGAIWELWEWILK SEQ ID NO: 520 CGIFEAIWELWEWILK SEQ ID NO: 521 CGLFEAIEGFIENGWEGMIDGWYGK(stearyl) SEQ ID NO: 522 (stearyl)GLFEAIEGFIENGWEGMIDGWYGC SEQ ID NO: 523 CFLE-Aib-LWKLLEHLL SEQ ID NO: 524 CFLE-Aib-LWELLEHLL SEQ ID NO: 525 CFLEALWE-Aib-LEHLL SEQ ID NO: 526 CFLE-Aib-LWE-Aib-LEHLL SEQ ID NO: 527 CFLE-Aib-LWEALEKLF SEQ ID NO: 528 (stearyl)IFGAIAGFIKNIWEGLIC SEQ ID NO: 529 CIFGAIAGFIKNIWEGLIK(stearyl) SEQ ID NO: 530 (stearyl)FFGAIWEFIKSILC SEQ ID NO: 531 CFFGAIWEFIKSILK(stearyl) SEQ ID NO: 532 (stearyl)FFGAIWEFIHSILC SEQ ID NO: 533 CFFGAIWEFIHSILK(stearyl) SEQ ID NO: 534 (stearyl)GIFEAIAGLLKNIFKC SEQ ID NO: 535 CGIFEAIAGLLKNIFK(stearyl) SEQ ID NO: 536 CGIFEAIAGLLKNIFKK(stearyl) SEQ ID NO: 537 (stearyl)IFGAIAGFIKNILKGLC SEQ ID NO: 538 CIFGAIAGFIKNILKGLK(stearyl) SEQ ID NO: 539 CIFGAIAGFIKNILKGL SEQ ID NO: 540 CGLFGEIEELIEEGLENLIDWWNS SEQ ID NO: 541 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 542 CGFFGEIAELIEEGLKNLIDWWNG SEQ ID NO: 543 CGLFEAIEGFIENGWKGMIDGWYGYGRKKRRQRR SEQ ID NO: 544 CGLFEAIEGFIEWGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 545 CGLFELIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 546 CIFGAIAGFIKNIWEGLI SEQ ID NO: 547 CGLFGEIEELIEEGLENLIDWWNG SEQ ID NO: 548 CGLFEEIEGFIENGWEGLIDWWYGYGHKKGGQHR SEQ ID NO: 549 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRRK(stearyl) SEQ ID NO: 550 CGLFEALLELLESLWELLEAYGRKKRRQRR SEQ ID NO: 551 CGLFEALLELLESLWELLEAYGRKKRRQRR SEQ ID NO: 552 CFFGAIWEFIRNILEGF SEQ ID NO: 553 CFFGAIWEFIRNILEGFK(stearyl) SEQ ID NO: 554 CIFGAIAGFIKNIWEGLIK(lauryl) SEQ ID NO: 555 (lauryl)FFGAIWEFIKSILC SEQ ID NO: 556 CFFGAIWEFIKSILK(lauryl) SEQ ID NO: 557 (lauryl)FFGAIWEFIHSILC SEQ ID NO: 558 CFFGAIWEFIHSILK(lauryl) SEQ ID NO: 559 (lauryl)GIFEAIAGLLKNIFKC SEQ ID NO: 560 CGIFEAIAGLLKNIFK(lauryl) SEQ ID NO: 561 CFFGAIWEFIRNILEGFK(lauryl) SEQ ID NO: 562 (lauryl)GLFEAIEGFIENGWEGMIDGWYGC SEQ ID NO: 563 CGLFEAIEGFIENGWEGMIDGWYGK(lauryl) SEQ ID NO: 564 CGKFTIVFPHNQKGNWKNVPSNYHYK(stearyl) SEQ ID NO: 565 CMDGTLFPGDDDLAIPATEFFSTKAK(stearyl) SEQ ID NO: 566 CNPVENYIDEVLNEVLVVPNINSSNK(stearyl) SEQ ID NO: 567 CVTPHHVLVDEYTGEWVDSQFK(stearyl) SEQ ID NO: 568 CIFGIDDLIIGLLFVAIVEAGIGGYLLGSK(stearyl) SEQ ID NO: 569 CGAAIGLAWIPYFGPAAEK(stearyl) SEQ ID NO: 570 CFAGVVLAGAALGVATAAQITAGIALHK(stearyl) SEQ ID NO: 571 CFLGFLLGVGSAIASGIAVSKVLHLK(stearyl) SEQ ID NO: 572 CFFGAVIGTIALGVATSAQITAGIALAK(stearyl) SEQ ID NO: 573 CFFGAVIGTIALGVATAAQITAGIALAK(stearyl) SEQ ID NO: 574 GLFEAIAGFIENGGWEGMIDGGGK(stearyl) SEQ ID NO: 575 GLFKAIAKFIKGGWKGLIKGWYGK(stearyl) SEQ ID NO: 576 GLFHAIAHFIHGGWHGLIHGWYGK(stearyl) SEQ ID NO: 577 CGLFEAIAEFIENGWEGLIEGWYGK(stearyl) SEQ ID NO: 578 CGFFGAIAGFLEGGWEGMIAGWHGK(stearyl) SEQ ID NO: 579 CFAGVVIGLAALGVATAAQVTAAVALVKK(stearyl) SEQ ID NO: 580 CAVGIVGAMFLGFLGAAGSTMGAVSLTLTVQAK(stearyl) SEQ ID NO: 581 CGVFVLGFLGFLATAGSAMGARSLTLSAK(stearyl) SEQ ID NO: 582 CVPFVLGFLGFLGAAGTAMGAAATALTVK(stearyl) SEQ ID NO: 583 CAVPVAVWLVSALAMGAGVAGGITGSMSLASGK(stearyl) SEQ ID NO: 584 CGLASTLTRWAHYNALIRAFK(stearyl) SEQ ID NO: 585 CGPVEDAITAAIGRVADTVGTK(stearyl) SEQ ID NO: 586 CGLGQMLESMIDNTVREVGGAK(stearyl) SEQ ID NO: 587 CGLFEAIEGFIENGWEGMIDGWYGFK(stearyl) SEQ ID NO: 588 (D)-(cgl)FEAIEGFIENGWEGMIDGWYGYGRKKRR(D)-(qrr) SEQ ID NO: 589 CG(lf)LEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 590 CIFGIDDLIIGLLFVAIVEAGIGGYLLGS(stearyl) SEQ ID NO: 591 CVTVLALGALAGVGVG(stearyl) SEQ ID NO: 592 CLLGRRGWEVLKYWWNLLQYWSQEL(stearyl) SEQ ID NO: 593 CGIFEAIAGLLKNIFD SEQ ID NO: 594 CGIFEAIAGLLKNIFE SEQ ID NO: 595 CGIFEAIAGLLKNIFR SEQ ID NO: 596 CGIFEAIAGLLKNIFH SEQ ID NO: 597 CGIFEAIAGLLKNIFO (O = ORNITHINE) SEQ ID NO: 598 CGIFEAIAGLLKNIFN SEQ ID NO: 599 CGIFEAIAGLLKNIFCit (Cit = citrulline) SEQ ID NO: 600 CGIFGAIWGLLKNIFK SEQ ID NO: 601 CIFEAIAGLLKNIFK SEQ ID NO: 602 CFFEAIAGLLKNIFK SEQ ID NO: 603 CGFFEAIAGLLKNIFK SEQ ID NO: 604 CGIFEAIAGLLKNIFKG SEQ ID NO: 605 CGIFEAIAGLLKNIFKGL SEQ ID NO: 606 CGIFEAIAGLLKNIFKGLI SEQ ID NO: 607 CGIFEAIAGLLKNIFKGLID SEQ ID NO: 608 CGIFEAIAGLLKNIFKGLIDG SEQ ID NO: 609 CGIFEAIAGLLKNIFKGLIDGF SEQ ID NO: 610 CGIFEAIAGLLKNIFKGLIDGWYG SEQ ID NO: 611 CGIFEAIAGLLKNIFK all(D) SEQ ID NO: 612 CGIFEAIAGLLKSILK SEQ ID NO: 613 CGIFEAIAGLLKNIFKA SEQ ID NO: 614 CGIFEAIAGLLKNIFKL SEQ ID NO: 615 CGIFEAIAGLLKNIFKW SEQ ID NO: 616 CGIFEAIAGLLKNIFKF SEQ ID NO: 617 CGIFEAIAGLLKNAFK SEQ ID NO: 618 CGIFGAIAGLLKNAFK SEQ ID NO: 619 CGIFEAIAGLLONIFO (O = Ornithine) SEQ ID NO: 620 CGIFEAIAGLLKNIFKGIFEAIAGLLKNIFK SEQ ID NO: 621 CGIFEAIAGLLKNIFKFFGAIWEFIHSIL SEQ ID NO: 622 CFFGAIWEFIHSILGIFEAIAGLLKNIFK SEQ ID NO: 623 CFFGAIWEFIHSILFFGAIWEFIHSIL SEQ ID NO: 624 CFFGAIWEFIHSILGFFGAIWEFIHSIL SEQ ID NO: 625 CGIFEAIAGLLKNIFKGIFEAIAGLLKNIFK SEQ ID NO: 626 CGIFEAIAGLLKNIFKFFGAIWEFIHSIL SEQ ID NO: 627 CFFGAIWEFIHSILGIFEAIAGLLKNIFK SEQ ID NO: 628 CGLFHALLHLLHSLWHLLLEA SEQ ID NO: 629 CGLFHALLHLLHSLWHLLLEAK(stearyl) SEQ ID NO: 630 CGLFHALLHLLHSLWHLLLEAK(stearyl) SEQ ID NO: 631 (stearyl)GLFHALLHLLHSLWHLLLEAC SEQ ID NO: 632 CFFGNIWEFIKSIL SEQ ID NO: 633 CFFGAIWLFIKSIL SEQ ID NO: 634 CFFGAIWNFIKSIL SEQ ID NO: 635 CFFGAIWGFIKSIL SEQ ID NO: 636 CFLGALFKALSKLL SEQ ID NO: 637 CFLGALFHALSKLL SEQ ID NO: 638 CFLGALFKALSHLL SEQ ID NO: 639 CFLGALFHALSHLL SEQ ID NO: 640 FLGALFKALSKLLC SEQ ID NO: 641 FLGALFHALSKLLC SEQ ID NO: 642 FLGALFKALSHLLC SEQ ID NO: 643 FLGALFHALSHLLC SEQ ID NO: 644 CFLGALFKALKSLL SEQ ID NO: 645 CFLGALFHALKSLL SEQ ID NO: 646 CFLGALFKALHSLL SEQ ID NO: 647 CFLGALFHALHSLL SEQ ID NO: 648 FLGALFKALKSLLC SEQ ID NO: 649 FLGALFHALKSLLC SEQ ID NO: 650 FLGALFKALHSLLC SEQ ID NO: 651 FLGALFHALHSLLC SEQ ID NO: 652 CGIFGAIAGFIKNIWKGLIDW SEQ ID NO: 653 CGLFEAIEGFIENGWEG-Nle-IDGWYGYGRKKRRQRR SEQ ID NO: 654 CGLFEAIEGFIENGLKGLIDWWYGYGRKKRRQRR SEQ ID NO: 655 CGLFEAIEGFIENAWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 656 CGLFEAIEGFIENGWEGMIDLWYGYGRKKRRQRR SEQ ID NO: 657 CRLLRLLLRLWRRLLRLLR SEQ ID NO: 658 CGIFGAIEGFIENGWKGLIDAWYGYRKKRRQRR SEQ ID NO: 659 CFFGAIWEFAHGIL SEQ ID NO: 660 CFFGAIWEFARGILEGF SEQ ID NO: 661 FFGAIWEFAHGILC SEQ ID NO: 662 FFGAIWEFARGILEGFC SEQ ID NO: 663 CFFGAIWEFAHSIL SEQ ID NO: 664 FFGAIWEFAHSILC SEQ ID NO: 665 CFFGAIWEFARSILK SEQ ID NO: 666 FFGAIWEFARSILKC SEQ ID NO: 667 CGIFEAIAGLAKNIFK SEQ ID NO: 668 GIFEAIAGLAKNIFKC SEQ ID NO: 669 CGIFEAIAGLAKNIFH SEQ ID NO: 670 CGIFEAIAGLAHNIFH SEQ ID NO: 671 CGIFEAIAGLAHNIFK SEQ ID NO: 672 GIFEAIAGLAKNIFHC SEQ ID NO: 673 GIFEAIAGLAHNIFHC SEQ ID NO: 674 CFLGALWKALSKLL SEQ ID NO: 675 CFLGALWHALSKLL SEQ ID NO: 676 CFLGALWKALSHLL SEQ ID NO: 677 CFLGALWHALSHLL SEQ ID NO: 678 FLGALWKALSKLLC SEQ ID NO: 679 FLGALWHALSKLLC SEQ ID NO: 680 FLGALWKALSHLLC SEQ ID NO: 681 FLGALWHALSHLLC SEQ ID NO: 682 CGIFGAIAGLLKNAFK SEQ ID NO: 683 CIFEAIAGLLKNAFK SEQ ID NO: 684 CIFGAIAGLLKNAFK SEQ ID NO: 685 CIFEAIWEFIKNIW SEQ ID NO: 686 CIFEAIAEFIKNIW SEQ ID NO: 687 CIFGAIWEFIKNIW SEQ ID NO: 688 CIFGAIAEFIKNIW SEQ ID NO: 689 CGIFGIAIGFKINIW SEQ ID NO: 690 CGIFEAIAGLLHNIFK SEQ ID NO: 691 CGIFEAIWGLLHNIFK SEQ ID NO: 692 CGFFEAIAGLLHNIFK SEQ ID NO: 693 CGIFEAIAALLKNIFK SEQ ID NO: 694 CGIFEAIEGLLKNIFK SEQ ID NO: 695 CGIFEAIAGFFKNIFK SEQ ID NO: 696 CGIFEAIAGWWKNIFK SEQ ID NO: 697 CGIFEAIAGLLKNIWK SEQ ID NO: 698 CGIFEAIAELLKNIFK SEQ ID NO: 699 CGIFGAIAGLLKSALK SEQ ID NO: 700 CGIFEAIAGLLKSIWK SEQ ID NO: 701 CGIFEAIAGLLKSILK SEQ ID NO: 702 CGIFEAIAGLLKNIFKGLIDA SEQ ID NO: 703 CGIFEAIAGLLKNIFKGLIDAF SEQ ID NO: 704 CGIFEAIAGLLKNIFKGLIDAWYG SEQ ID NO: 705 CGIFEAIAGLLKNIFKGLIDAWYGF SEQ ID NO: 706 CGIFEAIAGLLKNIFKGLIDGWYGF SEQ ID NO: 707 CGIFEAIAGLLKNIFKGLIDW SEQ ID NO: 708 CGIFEAIAGLLKNIFKGLIDWF SEQ ID NO: 709 CGIFEAIAGLLKNIFKGLIDWWYG SEQ ID NO: 710 CGIFEAIAGLLKNIFKGLIDWWYGF SEQ ID NO: 711 CGIFELIAGLLKNIFK SEQ ID NO: 712 CGIFEAIAGLLKWIFK SEQ ID NO: 713 CGIFELIAGLLKWIFK SEQ ID NO: 714 CGIFELIAGLLKNIFKG SEQ ID NO: 715 CGIFEAIAGLLKWIFKG SEQ ID NO: 716 CGIFELIAGLLKWIFKG SEQ ID NO: 717 CGLFEALLGLLESLWK SEQ ID NO: 718 CGIFEAIAELLKNIFK SEQ ID NO: 719 CGIFEALLGLLKSLWK SEQ ID NO: 720 CGIFEALLELLKSLWK SEQ ID NO: 721 CGIFEAIAGLLKNIFK SEQ ID NO: 722 CEIFEAIAGLLKNIFK SEQ ID NO: 723 CEIFGAIAGLLKNIFK SEQ ID NO: 724 CGLFEAIAGLLKNLFK SEQ ID NO: 725 CGIWEAIAGLLKNIWK SEQ ID NO: 726 CGLFGAIAGLLKNLFK SEQ ID NO: 727 CGIWGAIAGLLKNIWK SEQ ID NO: 728 CGIFDAIAGLLKNIFK SEQ ID NO: 729 CGIFDAIWGLLKNIFK SEQ ID NO: 730 CGIFGGIGGLLKNIFK SEQ ID NO: 731 CAIFAAIAALLKNIFK SEQ ID NO: 732 CGIFEAIAGLLKNIF SEQ ID NO: 733 CGIFEAIAGLLKNI SEQ ID NO: 734 CGIFEAIAGLLKN SEQ ID NO: 735 CGIFEAIAGLLK SEQ ID NO: 736 CVIFEAIAGLLKNIFK SEQ ID NO: 737 CSIFEAIAGLLKNIFK SEQ ID NO: 738 CGIFEEIAGLLKNIFK SEQ ID NO: 739 CGIFEEIWGLLKNIFK SEQ ID NO: 740 CGIFEAIEELLKNIFK SEQ ID NO: 741 CGIFEAIAGLWKNIFK SEQ ID NO: 742 CGIFEAIAGLLENIFK SEQ ID NO: 743 CGIFEAIAGLLWNIFK SEQ ID NO: 744 CGIFEAIAGLLKEIFK SEQ ID NO: 745 CGIFEAIAGLLKNILK SEQ ID NO: 746 CGIFEAIAGLLRNIFK SEQ ID NO: 747 CGIFEAIAGLLKSIFK SEQ ID NO: 748 CGIFEAIAGLLKNILK SEQ ID NO: 749 CGFFGAIWEFIKSILK SEQ ID NO: 750 CGFFEAIWEFIKSILK SEQ ID NO: 751 CGFFGAIWGLLKSILK SEQ ID NO: 752 CGFFEAIWGLLKSILK SEQ ID NO: 753 CGFFEAIAGLLKSILK SEQ ID NO: 754 CGFFGAIAGLLKSILK SEQ ID NO: 755 CGIFEAIAGLLKNIFEGLI SEQ ID NO: 756 CGIFEAIWGLLKNIFKGLI SEQ ID NO: 757 CGIFEAIWGLLKNIFEGLI SEQ ID NO: 758 CGIFEAIAGLLKNILKGLIDGWYG SEQ ID NO: 759 CGIFGAIAGLLKNILKGLIDGWYG SEQ ID NO: 760 CGIFGAIAGLLKNIFKGLIDGWYG SEQ ID NO: 761 CGIFGAIWELWEWILK SEQ ID NO: 762 CGIFEAIWELWEWILK SEQ ID NO: 763 CIFGAIWELWEWILK SEQ ID NO: 764 CIFEAIWELWEWILK SEQ ID NO: 765 CGIFEAIAELWKNIFK SEQ ID NO: 766 CGIFEAIAELWENIFK SEQ ID NO: 767 CGIFEAIAELWKWIFK SEQ ID NO: 768 CGIFEAIAELWEWIFK SEQ ID NO: 769 CGIFEAIAGLLKNILKGLIDWWYG SEQ ID NO: 770 CGIFGAIAGLLKNILKGLIDWWYG SEQ ID NO: 771 CGIFGAIAGLLKNIFKGLIDWWYG SEQ ID NO: 772 CGIFEAIAGLLKNILKGLIDGWYGF SEQ ID NO: 773 CGIFGAIAGLLKNILKGLIDGWYGF SEQ ID NO: 774 CGIFGAIAGLLKNIFKGLIDGWYGF SEQ ID NO: 775 CGIFGAIAELLEKIFE SEQ ID NO: 776 CGIFEAIAELLEKIFE SEQ ID NO: 777 CGFIGAIAELLEKIFE SEQ ID NO: 778 CGIFGAIAELLEKIFK SEQ ID NO: 779 CGIFEAIAELLEKIFK SEQ ID NO: 780 CGFIGAIAELLEKIFK SEQ ID NO: 781 CGLFHALLHLLHSLWHLLLEA SEQ ID NO: 782 GLFHALLHLLHSLWHGLLEAC SEQ ID NO: 783 GFFHAFFHFFHSFWHGFFEAC SEQ ID NO: 784 GLFHALLHLLHSLWHLLLEAC SEQ ID NO: 785 CGLFHALLHLLHSLWHGLLEAK(stearyl) SEQ ID NO: 786 CGFFHAFFHFFHSFWHGFFEAK(stearyl) SEQ ID NO: 787 CGLFHALLHLLHSLWHLLLEAK(stearyl) SEQ ID NO: 788 (stearyl)GLFHALLHLLHSLWHGLLEAC SEQ ID NO: 789 (stearyl)GFFHAFFHFFHSFWHGFFEAC SEQ ID NO: 790 (stearyl)GLFHALLHLLHSLWHLLLEAC SEQ ID NO: 791 CGFFHAFFHFFHSFWHFFFEA SEQ ID NO: 792 CGFFHAFFHFFHSFWHLFFEA SEQ ID NO: 793 CGLFHALLHLLHSLWHGLLEW SEQ ID NO: 794 CGLFHALLHLLHSLWHLLLEW SEQ ID NO: 795 CGFFHAFFHFFHSFWHGFFEW SEQ ID NO: 796 CFFGAIWEFAKSIL SEQ ID NO: 797 CFFGAIWEFAHSIL SEQ ID NO: 798 CFFGAIWEFAHGIL SEQ ID NO: 799 CFFGAIWEFIHSILK SEQ ID NO: 800 CFFGAIWEFIHSILH SEQ ID NO: 801 CFFGAIWEFIHSILD SEQ ID NO: 802 CFFGAIWEFIHSILR SEQ ID NO: 803 CFFGAIWEFIHSILO SEQ ID NO: 804 CFFGAIAEFIHSIL SEQ ID NO: 805 CIFGAIWEFIHSIL SEQ ID NO: 806 CGIFGAIWEFIHSIL SEQ ID NO: 807 CFFGAIWEFIHSILE SEQ ID NO: 808 CFFGAIWEFIHSILEG SEQ ID NO: 809 CFFGAIWEFIHSILEGL SEQ ID NO: 810 CFFGAIWEFIHSILEGLI SEQ ID NO: 811 CFFGAIWEFIHSILEGLID SEQ ID NO: 812 CFFGAIWEFIHSILEGLIDG SEQ ID NO: 813 CFFGAIWEFIHSILEGLIEA SEQ ID NO: 814 CFFGAIWEFIHSILEGLIDW SEQ ID NO: 815 CFFGAIWEFIHSILEGLIDGWYG SEQ ID NO: 816 CFFGAIWEFIHSILEGLIDGWYGF SEQ ID NO: 817 FFGAIWEFIHSILC SEQ ID NO: 818 CFWGAIWEFIHSIL SEQ ID NO: 819 CFFGAIWEFIHSILKGLIDW SEQ ID NO: 820 CAFGKIWEFAHSIL SEQ ID NO: 821 CAFGKIWEFIHSIL SEQ ID NO: 822 CFFGKIWEFIHSIL SEQ ID NO: 823 CAFGAIWEFIHSIL SEQ ID NO: 824 CAFGAIWEFAHSIL SEQ ID NO: 825 CGFFGAIAGLLHNIFK SEQ ID NO: 826 CFFGAIAGLLHNIFK SEQ ID NO: 827 CGFFEAIEGLLHNIFK SEQ ID NO: 828 CFFEAIAGLLHNIFK SEQ ID NO: 829 CFFEAIWGLLHNIFK SEQ ID NO: 830 CGFFGAIAELLHNIFK SEQ ID NO: 831 CFFGAIAELLHNIFK SEQ ID NO: 832 CGFFEAIAELLHNIFK SEQ ID NO: 833 CFFEAIAELLHNIFK SEQ ID NO: 834 CFFGAIWELLHNIFK SEQ ID NO: 835 CFFEAIWELLHNIFK SEQ ID NO: 836 CFFGAIWEFIHSILFFGAIWEFIHSIL SEQ ID NO: 837 CFFGAIWEFIHSILGGGFFGAIWEFIHSIL SEQ ID NO: 838 CFFGAIWEFIHSILGFFGAIWEFIHSIL SEQ ID NO: 839 GGLFEALLELLESLWELLLEW SEQ ID NO: 840 GGFFEAFFEFFESFWEFFFEA SEQ ID NO: 841 GGLFEALLELLESLWEGLLEA SEQ ID NO: 842 CGLFHALLHLLHSLWHLLLHA SEQ ID NO: 843 CGLFEALLHLLHSLWHLLLEA SEQ ID NO: 844 CGLFEALLELLHSLWHLLLEA SEQ ID NO: 845 CGLFEALLHLLESLWHLLLEA SEQ ID NO: 846 CGLFEALLHLLHSLWELLLEA SEQ ID NO: 847 CGLFHALLELLHSLWHLLLEA SEQ ID NO: 848 CGLFHALLHLLESLWHLLLEA SEQ ID NO: 849 CGLFHALLHLLHSLWELLLEA SEQ ID NO: 850 CGLFHALLELLESLWHLLLEA SEQ ID NO: 851 CGLFHALLELLHSLWELLLEA SEQ ID NO: 852 CGLFHALLHLLESLWELLLEA SEQ ID NO: 853 CGLFEALLHLLESLWELLLEA SEQ ID NO: 854 CGLFEALLELLHSLWELLLEA SEQ ID NO: 855 CGLEALLELLESLWHLLLEA SEQ ID NO: 856 CGLFHALLELLESLWELLLEA SEQ ID NO: 857 CFFGAIWEFIHSILHLLLEA SEQ ID NO: 858 CFFGAIWEFIHSILKLLLEA SEQ ID NO: 859 CGFFGAIWEFIHSILGFFGAIWEFIHSIL SEQ ID NO: 860 CFFGAIWEFAHSILFFGAIWEFAHSIL SEQ ID NO: 861 CFFGAIWEFAHSILGFFGAIWEFAHSIL SEQ ID NO: 862 CGFFGAIWEFAHSILGFFGAIWEFAHSIL SEQ ID NO: 863 CFFGAIWEFIHSILGLFEAIEGFIENGWEGMIDG SEQ ID NO: 864 CFFGAIWEFIHSILGLFEAIEGFIENGWEGMIDGWYG SEQ ID NO: 865 CFFGAIWEFIHSILGLFEAIEGFIENGWEGMIDGWYGF SEQ ID NO: 866 CFFGALLEFIHSILELLLEA SEQ ID NO: 867 CGLFGALLEFIHSILELLLEA SEQ ID NO: 868 CGFFGALLEFIHSILELLLEA SEQ ID NO: 869 CFFGALLEFIHSLWELLLEA SEQ ID NO: 870 CGLFGALLEFIHSLWELLLEA SEQ ID NO: 871 CGFFGALLEFIHSLWELLLEA SEQ ID NO: 872 CIFGAIAGFIKNIWK(stearyl) SEQ ID NO: 873 (stearyl) IFGAIAGFIKNIWC SEQ ID NO: 874 CFFGAIWEFIKSILK(stearyl) SEQ ID NO: 875 (stearyl)FFGAIWEFIKSILC SEQ ID NO: 876 CFFGAIWEFIHSILK(stearyl) SEQ ID NO: 877 (stearyl)FFGAIWEFIHSILC SEQ ID NO: 878 CIFGAIAGFIKNIWEGLIK(stearyl) SEQ ID NO: 879 (stearyl)IFGAIAGFIKNIWEGLIC SEQ ID NO: 880 (stearyl)IFGAIAGFIKNILKGLC SEQ ID NO: 881 (stearyl)GIFGAIAGFIKNILKGLC SEQ ID NO: 882 CIFGAIAGFIKNILKGLK(stearyl) SEQ ID NO: 883 CGLFGAIAGFIVNGWVGMIDG SEQ ID NO: 884 CGLFGAIAGFIVNGWVGMIDGWYG SEQ ID NO: 885 CGLFEAIEGFIVNGWVGMIDGWYG SEQ ID NO: 886 CGLFGAIAGFIVNGWVGMIDGWYGF SEQ ID NO: 887 CGLFEAIEAGFIVNGWVGMIDGWYGF SEQ ID NO: 888 CGLFGAIAGFIVNGWVGMIDGWYGK(stearyl) SEQ ID NO: 889 CGLFEAIEGFIVNGWVGMIDGWYGK(stearyl) SEQ ID NO: 890 (stearyl)GLFGAIAGFIVNGWVGMIDGWYGC SEQ ID NO: 891 (stearyl)GLFEAIEGFIVNGWVGMIDGWYGC SEQ ID NO: 892 (stearyl)GLFGAIAGFIVNGWVGMIDGWYGFC SEQ ID NO: 893 (stearyl)GLFEAIEAGFIVNGWVGMIDGWYGFC SEQ ID NO: 894 CFFGAIWGLLHSILH SEQ ID NO: 895 CFFGAIWELLHSIL SEQ ID NO: 896 CFFGAIWELLHSILH SEQ ID NO: 897 CFFGAIWGLLHSILK SEQ ID NO: 898 CFFGAIWELLHSILK SEQ ID NO: 899 CGLFGALLHLLHSLWELLLEA SEQ ID NO: 900 CGLFGALLELLHSLWELLLEA SEQ ID NO: 901 CFFGAIWEFIHSILELLLEA SEQ ID NO: 902 CFFGAIWEFIHSILHGLLEA SEQ ID NO: 903 CFFGAIWEFIHSILEGLLEA SEQ ID NO: 904 CGFFGAIWEFIHSILHLLLEA SEQ ID NO: 905 CGFFGAIWEFIHSILELLLEA SEQ ID NO: 906 CGFFGAIWEFIHSILHGLLEA SEQ ID NO: 907 CGFFGAIWEFIHSILEGLLEA SEQ ID NO: 908 CGFFGAIAGLLHSIL SEQ ID NO: 909 CGFFGAIWGLLHSIL SEQ ID NO: 910 CGFFGALLGLLHSIL SEQ ID NO: 911 CFFGAIWEFAKSAL SEQ ID NO: 912 CIFGAIAGFIHNILKGL SEQ ID NO: 913 CFFGAIAGFIKNILKGL SEQ ID NO: 914 CIFGAIWGFIKNILKGL SEQ ID NO: 915 CIFGAIWGFIHNILKGL SEQ ID NO: 916 CIFGAIAGLLKNILKGL SEQ ID NO: 917 CIFGAIAGLLHNILKGL SEQ ID NO: 918 CIFEAIAGFIKNILKGL SEQ ID NO: 919 CIFEAIAGFIHNILKGL SEQ ID NO: 920 CGNFGEIAELIEEGLKNLIDWWNG SEQ ID NO: 921 CGFFGEIAELIEEGLENLIDWWNG SEQ ID NO: 922 CGNFGEIEELIEEGLKNLIDWWNG SEQ ID NO: 923 CGNFGEIAELIEEGLENLIDWWNG SEQ ID NO: 924 CGFFGEIEELIEENGENLIDWWNG SEQ ID NO: 925 CGFFGAIEELIEEGLKNLIDWWNG SEQ ID NO: 926 CGFFGAIAELIEEGLKNLIDWWNG SEQ ID NO: 927 CGFFGEIAELIEEGLKNLIDWWNGF SEQ ID NO: 928 GFFGEIAELIEEGLKNLIDWWNGC SEQ ID NO: 929 GNWWDILNKLGEEILEAIEGFFGC SEQ ID NO: 930 CGNWWDILNKLGEEILEAIEGFFG SEQ ID NO: 931 CGFLGEIAELIEEGLKNLIDWWNG SEQ ID NO: 932 CGFFGEIWELIEEGLKNLIDWWNG SEQ ID NO: 933 CGFFGEIAELWEEGLKNLIDWWNG SEQ ID NO: 934 CGFFGEIAELIWEGLKNLIDWWNG SEQ ID NO: 935 CGFFGEIAELIEWGLKNLIDWWNG SEQ ID NO: 936 CGFFGEIAELIEEGLRNLIDWWNG SEQ ID NO: 937 CGFFGEIAELIEEGLDNLIDWWNG SEQ ID NO: 938 CGFFGEIAELIEEGLKNLNDWWNG SEQ ID NO: 939 CGFFGEIEELIEEGLKNLIDWWNG SEQ ID NO: 940 CGFLGEIEELIEEGLKNLIDWWNG SEQ ID NO: 941 CGFFGLIEELIEEGLKNLIDWWNG SEQ ID NO: 942 CGFFGEIAELIEEGLKNLIDWWNGK(stearyl) SEQ ID NO: 943 (stearyl)GFFGEIAELIEEGLKNLIDWWNGC SEQ ID NO: 944 CFFGAIWEFAKSILK(stearyl) SEQ ID NO: 945 CGFFGAIWEFAKSIL SEQ ID NO: 946 CFFGKIWEFIKSILK(stearyl) SEQ ID NO: 947 (stearyl)FFGKIWEFIKSILC SEQ ID NO: 948 CFFGAIWEFIKSIAK(stearyl) SEQ ID NO: 949 (stearyl)FFGAIWEFIKSIAC SEQ ID NO: 950 (stearyl)FFGAIWEFAKSILC SEQ ID NO: 951 CFFGGIWEFIKSILK(stearyl) SEQ ID NO: 952 (stearyl)FFGGIWEFIKSILC SEQ ID NO: 953 CFFKAIWEFIKSILK(stearyl) SEQ ID NO: 954 (stearyl)FFKAIWEFIKSILC SEQ ID NO: 955 CFFGAIWEAIKSILK(stearyl) SEQ ID NO: 956 (stearyl)FFGAIWEAIKSILC SEQ ID NO: 957 CFFKAIWEFAKSIL SEQ ID NO: 958 CFFKAIWEFAHSIL SEQ ID NO: 959 CFFKAIWEFAKSILK(stearyl) SEQ ID NO: 960 (stearyl)FFKAIWEFAKSILC SEQ ID NO: 961 CFFKAIWEFAHSILK(stearyl) SEQ ID NO: 962 CGLFGEIAELIEEGLENLIDWWNG SEQ ID NO: 963 CGLFGEIEELIEEGLKNLIDWWNG SEQ ID NO: 964 CFFGAIWEFAKSILK(stearyl) SEQ ID NO: 965 CGLFGEIEELIEEGLKGLIDWWNG SEQ ID NO: 966 CGLFGEIAELIEEGLKNLIDWWNG SEQ ID NO: 967 CGLFGEIAELIEEGLEGLIDWWNG SEQ ID NO: 968 GLFGEIEELIEEGLENLIDWWNGC SEQ ID NO: 969 (stearyl)GLFGEIEELIEEGLENLIDWWNGC SEQ ID NO: 970 CGLFGEIEELIEEGLENLIDWWNGK(stearyl) SEQ ID NO: 971 CGNWWDILNELGEEILEEIEGFLG SEQ ID NO: 972 CALFGEIEELIEEGLENLIDWWNG SEQ ID NO: 973 CELFGEIEELIEEGLENLIDWWNG SEQ ID NO: 974 CSLFGEIEELIEEGLENLIDWWNG SEQ ID NO: 975 CNLFGEIEELIEEGLENLIDWWNG SEQ ID NO: 976 CVLFGEIEELIEEGLENLIDWWNG SEQ ID NO: 977 CGFFGEIEELIEEGLENLIDWWNG SEQ ID NO: 978 CGVFGEIEELIEEGLENLIDWWNG SEQ ID NO: 979 CGIFGEIEELIEEGLENLIDWWNG SEQ ID NO: 980 CGWFGEIEELIEEGLENLIDWWNG SEQ ID NO: 981 CGYFGEIEELIEEGLENLIDWWNG SEQ ID NO: 982 CGLLGEIEELIEEGLENLIDWWNG SEQ ID NO: 983 CGLVGEIEELIEEGLENLIDWWNG SEQ ID NO: 984 CGLIGEIEELIEEGLENLIDWWNG SEQ ID NO: 985 CGLWGEIEELIEEGLENLIDWWNG SEQ ID NO: 986 CGLYGEIEELIEEGLENLIDWWNG SEQ ID NO: 987 CGLFEEIEELIEEGLENLIDWWNG SEQ ID NO: 988 CGLFAEIEELIEEGLENLIDWWNG SEQ ID NO: 989 CGLFNEIEELIEEGLENLIDWWNG SEQ ID NO: 990 CGLFSEIEELIEEGLENLIDWWNG SEQ ID NO: 991 CGLFGAIEELIEEGLENLIDWWNG SEQ ID NO: 992 CGLFGDIEELIEEGLENLIDWWNG SEQ ID NO: 993 CGLFGNIEELIEEGLENLIDWWNG SEQ ID NO: 994 CGLFGSIEELIEEGLENLIDWWNG SEQ ID NO: 995 CGLFGELEELIEEGLENLIDWWNG SEQ ID NO: 996 CGLFGEVEELIEEGLENLIDWWNG SEQ ID NO: 997 CGLFGEFEELIEEGLENLIDWWNG SEQ ID NO: 998 CGLFGEWEELIEEGLENLIDWWNG SEQ ID NO: 999 CGLFGEYEELIEEGLENLIDWWNG SEQ ID NO: 1000 CGLFGEIAELIEEGLENLIDWWNG SEQ ID NO: 1001 CGLFGEIGELIEEGLENLIDWWNG SEQ ID NO: 1002 CGLFGEILELIEEGLENLIDWWNG SEQ ID NO: 1003 CGLFGEIVELIEEGLENLIDWWNG SEQ ID NO: 1004 CGLFGEISELIEEGLENLIDWWNG SEQ ID NO: 1005 CGLFGEIEDLIEEGLENLIDWWNG SEQ ID NO: 1006 CGLFGEIENLIEEGLENLIDWWNG SEQ ID NO: 1007 CGLFGEIESLIEEGLENLIDWWNG SEQ ID NO: 1008 CGLFGEIEALIEEGLENLIDWWNG SEQ ID NO: 1009 CGLFGEIEGLIEEGLENLIDWWNG SEQ ID NO: 1010 CGLFGEIEEVIEEGLENLIDWWNG SEQ ID NO: 1011 CGLFGEIEEIIEEGLENLIDWWNG SEQ ID NO: 1012 CGLFGEIEEFIEEGLENLIDWWNG SEQ ID NO: 1013 CGLFGEIEEAIEEGLENLIDWWNG SEQ ID NO: 1014 CGLFGEIEEYIEEGLENLIDWWNG SEQ ID NO: 1015 CGLFGEIEEWIEEGLENLIDWWNG SEQ ID NO: 1016 CGLFGEIEELVEEGLENLIDWWNG SEQ ID NO: 1017 CGLFGEIEELLEEGLENLIDWWNG SEQ ID NO: 1018 CGLFGEIEELFEEGLENLIDWWNG SEQ ID NO: 1019 CGLFGEIEELAEEGLENLIDWWNG SEQ ID NO: 1020 CGLFGEIEELYEEGLENLIDWWNG SEQ ID NO: 1021 CGLFGEIEELWEEGLENLIDWWNG SEQ ID NO: 1022 CGLFGEIEELIDEGLENLIDWWNG SEQ ID NO: 1023 CGLFGEIEELINEGLENLIDWWNG SEQ ID NO: 1024 CGLFGEIEELISEGLENLIDWWNG SEQ ID NO: 1025 CGLFGEIEELIEDGLENLIDWWNG SEQ ID NO: 1026 CGLFGEIEELIEYGLENLIDWWNG SEQ ID NO: 1027 CGLFGEIEELIESGLENLIDWWNG SEQ ID NO: 1028 CGLFGEIEELIEQGLENLIDWWNG SEQ ID NO: 1029 CGLFGEIEELIENGLENLIDWWNG SEQ ID NO: 1030 CGLFGEIEELIEEALENLIDWWNG SEQ ID NO: 1031 CGLFGEIEELIEENLENLIDWWNG SEQ ID NO: 1032 CGLFGEIEELIEESLENLIDWWNG SEQ ID NO: 1033 CGLFGEIEELIEEQLENLIDWWNG SEQ ID NO: 1034 CGLFGEIEELIEEGWENLIDWWNG SEQ ID NO: 1035 CGLFGEIEELIEEGVENLIDWWNG SEQ ID NO: 1036 CGLFGEIEELIEEGIENLIDWWNG SEQ ID NO: 1037 CGLFGEIEELIEEGFENLIDWWNG SEQ ID NO: 1038 CGLFGEIEELIEEGAENLIDWWNG SEQ ID NO: 1039 CGLFGEIEELIEEGYENLIDWWNG SEQ ID NO: 1040 CGLFGEIEELIEEGLRNLIDWWNG SEQ ID NO: 1041 CGLFGEIEELIEEGLHNLIDWWNG SEQ ID NO: 1042 CGLFGEIEELIEEGLONLIDWWNG SEQ ID NO: 1043 CGLFGEIEELIEEGLDNLIDWWNG SEQ ID NO: 1044 CGLFGEIEELIEEGLKNLIDWWNG SEQ ID NO: 1045 CGLFGEIEELIEEGLEGLIDWWNG SEQ ID NO: 1046 CGLFGEIEELIEEGLEYLIDWWNG SEQ ID NO: 1047 CGLFGEIEELIEEGLEQLIDWWNG SEQ ID NO: 1048 CGLFGEIEELIEEGLESLIDWWNG SEQ ID NO: 1049 CGLFGEIEELIEEGLEALIDWWNG SEQ ID NO: 1050 CGLFGEIEELIEEGLE(Cit)LIDWWNG SEQ ID NO: 1051 CGLFGEIEELIEEGLENMIDWWNG SEQ ID NO: 1052 CGLFGEIEELIEEGLENFIDWWNG SEQ ID NO: 1053 CGLFGEIEELIEEGLENIIDWWNG SEQ ID NO: 1054 CGLFGEIEELIEEGLENWIDWWNG SEQ ID NO: 1055 CGLFGEIEELIEEGLENVIDWWNG SEQ ID NO: 1056 CGLFGEIEELIEEGLENYIDWWNG SEQ ID NO: 1057 CGLFGEIEELIEEGLEN(Nle)IDWWNG SEQ ID NO: 1058 CGLFGEIEELIEEGLENLIDWWNG SEQ ID NO: 1059 CGLFGEIEELIEEGLENLVDWWNG SEQ ID NO: 1060 CGLFGEIEELIEEGLENLFDWWNG SEQ ID NO: 1061 CGLFGEIEELIEEGLENLWDWWNG SEQ ID NO: 1062 CGLFGEIEELIEEGLENLYDWWNG SEQ ID NO: 1063 CGLFGEIEELIEEGLENLIEWWNG SEQ ID NO: 1064 CGLFGEIEELIEEGLENLINWWNG SEQ ID NO: 1065 CGLFGEIEELIEEGLENLISWWNG SEQ ID NO: 1066 CGLFGEIEELIEEGLENLIQWWNG SEQ ID NO: 1067 CGLFGEIEELIEEGLENLIDGWNG SEQ ID NO: 1068 CGLFGEIEELIEEGLENLIDAWNG SEQ ID NO: 1069 CGLFGEIEELIEEGLENLIDFWNG SEQ ID NO: 1070 CGLFGEIEELIEEGLENLIDLWNG SEQ ID NO: 1071 CGLFGEIEELIEEGLENLIDIWNG SEQ ID NO: 1072 CGLFGEIEELIEEGLENLIDVWNG SEQ ID NO: 1073 CGLFGEIEELIEEGLENLIDWGNG all (D) SEQ ID NO: 1074 CGLFGEIEELIEEGLENLIDWANG SEQ ID NO: 1075 CGLFGEIEELIEEGLENLIDWFNG SEQ ID NO: 1076 CGLFGEIEELIEEGLENLIDWING SEQ ID NO: 1077 CGLFGEIEELIEEGLENLIDWVNG SEQ ID NO: 1078 CGLFGEIEELIEEGLENLIDWYNG SEQ ID NO: 1079 CGLFGEIEELIEEGLENLIDWWQG SEQ ID NO: 1080 CGLFGEIEELIEEGLENLIDWWTG SEQ ID NO: 1081 CGLFGEIEELIEEGLENLIDWWSG SEQ ID NO: 1082 CGLFGEIEELIEEGLENLIDWWEG SEQ ID NO: 1083 CGLFGEIEELIEEGLENLIDWW(Cit)G SEQ ID NO: 1084 CGLFGEIEELIEEGLENLIDWWNA SEQ ID NO: 1085 CGLFGEIEELIEEGLENLIDWWNN SEQ ID NO: 1086 CGLFGEIEELIEEGLENLIDWWNS SEQ ID NO: 1087 CGLFGEIEELIEEGLENLIDWWNY SEQ ID NO: 1088 CGLFGEIEELIEEGLENLIDWWNW SEQ ID NO: 1089 CFFGAIWGLLHSIL SEQ ID NO: 1090 CFFGK(stearyl)IWEFIKSIL SEQ ID NO: 1091 CFFGK(stearyl)IWEFIHSIL SEQ ID NO: 1092 CFFK(stearyl)AIWEFIKSIL SEQ ID NO: 1093 CGFFGAIWGLLHSILK SEQ ID NO: 1094 CGFFEAIWGLLHSIL SEQ ID NO: 1095 CFFGAIWGLLKSIL SEQ ID NO: 1096 CGFFGAIWGLLKSIL SEQ ID NO: 1097 CFFEAIWGLLKSIL SEQ ID NO: 1098 CGFFEAIWGLLKSIL SEQ ID NO: 1099 CFFGAIWGLLHSILKGLIDWWNG SEQ ID NO: 1100 CFFGAIWGLLHSILKGLIDGWYG SEQ ID NO: 1101 CGIFGAIAGLLKNIFKG SEQ ID NO: 1102 CGIFGAIAGLLKNIFKA SEQ ID NO: 1103 CGIFGAIAGLLKNIFKL SEQ ID NO: 1104 CGIFGAIAGLLKNIFKW SEQ ID NO: 1105 CGIFGAIAGLLKNIFKF SEQ ID NO: 1106 CGIFGAIAGLLKNIFKN SEQ ID NO: 1107 CGIFGAIAGLLKNIFKE SEQ ID NO: 1108 CGIFGAIAGLLKNIFKS SEQ ID NO: 1109 CGIFGAIAGLLKNIFK(stearyl) SEQ ID NO: 1110 CGIFGAIAGLLKNIFKK(stearyl) SEQ ID NO: 1111 (stearyl)GIFGAIAGLLKNIFKC SEQ ID NO: 1112 CGIFGAIAGLLKNIFK(lauryl) SEQ ID NO: 1113 CGIFGAIAGLLKNIFKK(lauryl) SEQ ID NO: 1114 (lauryl)GIFGAIAGLLKNIFKC SEQ ID NO: 1115 CGIFGAIAGLLHNIFK SEQ ID NO: 1116 CGIFGAIAGLLONIFK SEQ ID NO: 1117 CGIFGAIAGLLRNIFK SEQ ID NO: 1118 CGIFGAIAGLLENIFK SEQ ID NO: 1119 CGIFGAIAGLLDNIFK SEQ ID NO: 1120 CGIFGAIAGLLKNIFH SEQ ID NO: 1121 CGIFGAIAGLLKNIFO SEQ ID NO: 1122 CGIFGAIAGLLKINFE SEQ ID NO: 1123 CGIFGAIAGLLKNIFD SEQ ID NO: 1124 CGIFGAIAGLLKNIFN SEQ ID NO: 1125 CGIFGAIAGLLNNIFK SEQ ID NO: 1126 CGIFGIAIGLLKNIFKGIFGAIAGLLKNIFK SEQ ID NO: 1127 CGIFGAIWGLLKNIFKG SEQ ID NO: 1128 CGIFGAIWGLLKNIFKA SEQ ID NO: 1129 CGIFGAIWGLLKNIFKL SEQ ID NO: 1130 CGIFGAIWGLLKNIFKW SEQ ID NO: 1131 CGIFGAIWGLLKNIFKF SEQ ID NO: 1132 CGIFGAIWGLLKNIFKN SEQ ID NO: 1133 CGIFGAIWGLLKNIFKE SEQ ID NO: 1134 CGIFGAIWGLLKNIFKS SEQ ID NO: 1135 CGIFGAIWGLLKNIFK(stearyl) SEQ ID NO: 1136 CGIFGAIWGLLKNIFKK(stearyl) SEQ ID NO: 1137 (stearyl)GIFGAIWGLLKNIFKC SEQ ID NO: 1138 CGIFGAIWGLLKNIFK(lauryl) SEQ ID NO: 1139 CGIFGAIWGLLKNIFKK(lauryl) SEQ ID NO: 1140 (lauryl)GIFGAIWGLLKNIFKC SEQ ID NO: 1141 CGIFGAIWGLLHNIFK SEQ ID NO: 1142 CGIFGAIWGLLONIFK SEQ ID NO: 1143 CGIFGAIWGLLRNIFK SEQ ID NO: 1144 CGIFGAIWGLLENIFK SEQ ID NO: 1145 CGIFGAIWGLLDNIFK SEQ ID NO: 1146 CGIFGAIWGLLKNIFH SEQ ID NO: 1147 CGIFGAIWGLLKNIFO SEQ ID NO: 1148 CGIFGAIWGLLKINFE SEQ ID NO: 1149 CGIFGAIWGLLKNIFD SEQ ID NO: 1150 CGIFGAIWGLLKNIFN SEQ ID NO: 1151 CGIFGAIWGLLNNIFK SEQ ID NO: 1152 CFFGAIWGLLKNIFK SEQ ID NO: 1153 CGFFGAIWGLLKNIFK SEQ ID NO: 1154 CIFGAIWGLLKNIFK SEQ ID NO: 1155 CGIFGAIWIGLLKNIFKGIFGAIWGLLKNIFK SEQ ID NO: 1156 CGIFGAIWGLLHNIFH SEQ ID NO: 1157 CGIFGAIWGLLONIFO SEQ ID NO: 1158 CGIFGAIAGLLHSILK SEQ ID NO: 1159 CGIFGAIWGLLHSILK SEQ ID NO: 1160 CGIFGAIAGLLHSIL SEQ ID NO: 1161 CGIFGAIWGLLHSIL SEQ ID NO: 1162 CGIFGAIWELLKNIFK SEQ ID NO: 1163 CGIFGAIWGLLHNIFHGIFGAIWGLLHNIFK SEQ ID NO: 1164 CGIFEAIWGLLHNIFHGIFEAIWGLLHNIFH SEQ ID NO: 1165 CGIFEAIWGLLKNIFHGIFEAIWGLLHNIFH SEQ ID NO: 1166 CGIFEAIWGLLKNIFKGIFEAIWELLKNIFH SEQ ID NO: 1167 CGIFEAIWGLLKNIFHGIFEAIWGLLKNIFH SEQ ID NO: 1168 CGLFEALLELLESLWELLLEAWNG SEQ ID NO: 1169 CGLFEALLELLESLWELLLEWWNG SEQ ID NO: 1170 CGLFGELEELLEEGLENLLDWWNG SEQ ID NO: 1171 CGLFGELEELLEEGLENLLEWWNG SEQ ID NO: 1172 CGLFGELEELLEEGWELLLEAWNG SEQ ID NO: 1173 CGLFGELEELLEEGWELLLEWWNG SEQ ID NO: 1174 CGLFGELEELLEEGWELLLDWWNG SEQ ID NO: 1175 CGLFGALLELLEEGLENLIDWWNG SEQ ID NO: 1176 CGLFEALLELLEEGLENLIDWWNG SEQ ID NO: 1177 CGLFEALLELLESLLENLIDWWNG SEQ ID NO: 1178 CGLFGELAELLEEGLENLLDWWNG SEQ ID NO: 1179 GLFGEIEELIEEGLENLIDWWNG SEQ ID NO: 1180 CFFGNIWEFIHSIL SEQ ID NO: 1181 CFFGAIWNFIHSIL SEQ ID NO: 1182 CFFGNIWNFIHSIL SEQ ID NO: 1183 CGIFGNIWNFIKNIFK SEQ ID NO: 1184 CGIFGNIWNLLKNIFK SEQ ID NO: 1185 CGIFGNIWGLLKNIFK SEQ ID NO: 1186 CGIFGNIWNFIKNIFH SEQ ID NO: 1187 CGIFGNIWNLLKNIFH SEQ ID NO: 1188 CGIFGNIWGLLKNIFH SEQ ID NO: 1189 CGIFENIWNFIKNIFK SEQ ID NO: 1190 CGIFENIWNFIKNIFH SEQ ID NO: 1191 CGIFENIWGLLKNIFK SEQ ID NO: 1192 CGIFENIWGLLKNIFH SEQ ID NO: 1193 CGIFENIWNLLKNIFK SEQ ID NO: 1194 CGIFENIWNLLKNIFH SEQ ID NO: 1195 CGLFGAIAGLLENIFENLIDWWNG SEQ ID NO: 1196 CGLFGAIAGLLNKIFKNLIDWWNG SEQ ID NO: 1197 CGLFGAIAGLLENIFKNLIDWWNG SEQ ID NO: 1198 CGLFGAIAGLLKNIFENLIDWWNG SEQ ID NO: 1199 CGLFGAIAGLLKNIFHNLIDWWNG SEQ ID NO: 1200 CLIGAILKVLATGLPTLISWIKNKRKQ SEQ ID NO: 1201 CGLLEEIEELLEEGLENLIDWWNG SEQ ID NO: 1202 CGLFEELEELLEEGLENLIDWWNG SEQ ID NO: 1203 CGLFEELEELLEEGLENLIEA SEQ ID NO: 1204 CGLFEELEELLEEGLENLIEAWNG SEQ ID NO: 1205 CGLFEELEELLEEGLENLIEW SEQ ID NO: 1206 CGLFEELEELLEEGLENLIEWWNG SEQ ID NO: 1207 CGLFEELEELLEEGLENLIDA SEQ ID NO: 1208 CGLFEELEELLEEGLENLIDAWNG SEQ ID NO: 1209 CGLFEELEELLEEGLENLIDW SEQ ID NO: 1210 CFLGALKFALKSLL SEQ ID NO: 1211 CFLGALHFALKSLL SEQ ID NO: 1212 CFLGALKFALHSLL SEQ ID NO: 1213 CFLGALHFALHSLL SEQ ID NO: 1214 FLGALKFALKSLLC SEQ ID NO: 1215 GFLGALKFALKSLLC SEQ ID NO: 1216 CGLFGELEELIEEGLENLLDWWNG SEQ ID NO: 1217 CGLFGEIEELLEEGLENLLDWWNG SEQ ID NO: 1218 CGLFGELEELLEEGLENLIDWWNG SEQ ID NO: 1219 CGLFGEIEELIEEGLENLMDWWNG SEQ ID NO: 1220 CGLFGEIEELIEEGLENLEDWWNG SEQ ID NO: 1221 CGLFGEIEELIEEGLENLDDWWNG SEQ ID NO: 1222 CGLFGEIEELIEEGLENLNDWWNG SEQ ID NO: 1223 CGLFGEIEELIEEGLENLSDWWNG SEQ ID NO: 1224 CGLFGEIEELIEEGLENLQDWWNG SEQ ID NO: 1225 CGLFGEIEELIEEGLENL-CIT-DWWNG SEQ ID NO: 1226 CGLFGEIEELIEELLENLIDWWNG SEQ ID NO: 1227 CGLFGEIEELIEEILENLIDWWNG SEQ ID NO: 1228 CGLFGEIEELIEEVLENLIDWWNG SEQ ID NO: 1229 CFLGALWKLLSHLL SEQ ID NO: 1230 CFLGALWKILSHLL SEQ ID NO: 1231 CFLGALWVKVLSHLL SEQ ID NO: 1232 CFLGALWKFLSHLL SEQ ID NO: 1233 CFLEALWKALSHLL SEQ ID NO: 1234 CFLHALWKALSHLL SEQ ID NO: 1235 CFLKALWKALSHLL SEQ ID NO: 1236 CFLNALWKALSHLL SEQ ID NO: 1237 CFLSALWKALSHLL SEQ ID NO: 1238 CFLQALWKALSHLL SEQ ID NO: 1239 CFLEALWEALSHLL SEQ ID NO: 1240 CFLGALWEALSHLL SEQ ID NO: 1241 CFLEALWKLLSHLL SEQ ID NO: 1242 CFLEALWEALEELL SEQ ID NO: 1243 CFLEELWEALEELL SEQ ID NO: 1244 CFLEALWEALEHLL SEQ ID NO: 1245 CFLEELWEALEHLL SEQ ID NO: 1246 CFLEELWELLEELL SEQ ID NO: 1247 CFLEELWELLEHLL SEQ ID NO: 1248 CGLFGEIEELLEEGLE-CIT-LIDWWNG SEQ ID NO: 1249 CGLFEEIEELLEEGLE-CIT-LIDWWNG SEQ ID NO: 1250 CGLFGEIAELLEEGLE-CIT-LIDWWNG SEQ ID NO: 1251 CGLFEEIAELLEEGLE-CIT-LIDWWNG SEQ ID NO: 1252 CGLFGEIEELLEEGLE-CIT-LVDWWNG SEQ ID NO: 1253 CGLFEEIEELLEEGLE-CIT-LVDWWNG SEQ ID NO: 1254 CGLFGEIAELLEEGLE-CIT-LVDWWNG SEQ ID NO: 1255 CGLFEEIAELLEEGLE-CIT-LVDWWNG SEQ ID NO: 1256 CGLFGEIEELLEEGLE-CIT-LIDWWNE SEQ ID NO: 1257 CGLFEEIEELLEEGLE-CIT-LIDWWNE SEQ ID NO: 1258 CGLFGEIAELLEEGLE-CIT-LIDWWNE SEQ ID NO: 1259 CGLFEEIAELLEEGLE-CIT-LIDWWNE SEQ ID NO: 1260 CGLFGEIEELLEEGLH-CIT-LIDWWNG SEQ ID NO: 1261 CGLFEEIEELLEEGLH-CIT-LIDWWNG SEQ ID NO: 1262 CGLFGEIAELLEEGLH-CIT-LIDWWNG SEQ ID NO: 1263 CGLFEEIAELLEEGLH-CIT-LIDWWNG SEQ ID NO: 1264 CGLFGEIEELLEEGLE-CIT-LVDWWNE SEQ ID NO: 1265 CGLFEEIEELLEEGLE-CIT-LVDWWNE SEQ ID NO: 1266 CGLFGEIAELLEEGLE-CIT-LVDWWNE SEQ ID NO: 1267 CGLFEEIAELLEEGLE-CIT-LVDWWNE SEQ ID NO: 1268 CFFKNIWEFIKSIL SEQ ID NO: 1269 CFFKNIWNFIKSIL SEQ ID NO: 1270 CFFKAIWEFIKSILE SEQ ID NO: 1271 CFFKAIWEFIKNIFK SEQ ID NO: 1272 CFFKAIWEFIKNIFKE SEQ ID NO: 1273 CFFKAIWELLKSIL SEQ ID NO: 1274 CFFKAIWGLLKSIL SEQ ID NO: 1275 CFFKAIWEFIKSILK SEQ ID NO: 1276 CFFKNIWGLLKSIL SEQ ID NO: 1277 CFFKAIWGLLKNIFK SEQ ID NO: 1278 CFFKAIWELLKNIFK SEQ ID NO: 1279 CFFKNIWGLLKNIFK SEQ ID NO: 1280 CFFKNIWELLKNIFK SEQ ID NO: 1281 CFFKAIWEFIRSIL SEQ ID NO: 1282 CFFKAIWEFIKSLL SEQ ID NO: 1283 CFFKAIWEFIKSAL SEQ ID NO: 1284 CFFKAIWEFIKSIF SEQ ID NO: 1285 CFFKALWEFLKSLL SEQ ID NO: 1286 CIFKAIWEFIKSIL SEQ ID NO: 1287 CFFKAIWEFIKSIW SEQ ID NO: 1288 CFFHAIWEFIKSIL SEQ ID NO: 1289 CFFEAIWEFIKSIL SEQ ID NO: 1290 CFFKAIAEFIKSIL SEQ ID NO: 1291 CFFKAIEEFIKSIL SEQ ID NO: 1292 CFFKAILEFIKSIL SEQ ID NO: 1293 CFFKAIFEFIKSIL SEQ ID NO: 1294 CFFKAIWGFIKSIL SEQ ID NO: 1295 CFFKAIWHFIKSIL SEQ ID NO: 1296 CFFKAIWKFIKSIL SEQ ID NO: 1297 CFFEAIWKFIKSIL SEQ ID NO: 1298 CFFKAIWELIKSIL SEQ ID NO: 1299 CFFKALWELLKSLL SEQ ID NO: 1300 CFFKAIWEAIKSIL SEQ ID NO: 1301 CFFKAIWEFLKSIL SEQ ID NO: 1302 CFFKAIWEFIHSIL SEQ ID NO: 1303 CFFKAIWEFIESIL SEQ ID NO: 1304 CFFKAIWEFIKNIL SEQ ID NO: 1305 CFFKAIWEFIKWIL SEQ ID NO: 1306 CFFKAIWEFIKEIL SEQ ID NO: 1307 CFFKAIWEFIKGIL SEQ ID NO: 1308 CFFKAIWEFIKSGL SEQ ID NO: 1309 CFFKAIWEFIKSII SEQ ID NO: 1310 CFFKAIWEFIK-CIT-IL SEQ ID NO: 1311 CFFKAIWEFIKSIA SEQ ID NO: 1312 CFFKAIWEFIKQIL SEQ ID NO: 1313 CGFFKAIWEFIKSIL SEQ ID NO: 1314 CFFKAIWEFIKSILKGLIDG SEQ ID NO: 1315 CFFKAIWEFIKSILKGLIDGWYG SEQ ID NO: 1316 CFFKAIWEFIKSILEGLIDG SEQ ID NO: 1317 CFFKAIWEFIKSILEGLIDGWYG SEQ ID NO: 1318 CFFKAIWEFIKNIFKGLIDG SEQ ID NO: 1319 CFFKAIWEFIKNIFKGLIDGWYG SEQ ID NO: 1320 CFFGNIWEFIKSILKGLIDG SEQ ID NO: 1321 CFFGNIWEFIKSILKGLIDGWYG SEQ ID NO: 1322 CFFGNIWEFIKSILEGLIDG SEQ ID NO: 1323 CFFGNIWEFIKSILEGLIDGWYG SEQ ID NO: 1324 CFFGNIWEFIKNIFKGLIDG SEQ ID NO: 1325 CFFGNIWEFIKNIFKGLIDGEYG SEQ ID NO: 1326 CFFKAIWGLLKSILKGLIDG SEQ ID NO: 1327 CFFKAIWGLLKSILKGLIDGWYG SEQ ID NO: 1328 CFFKAIWGLLKSILEGLIDG SEQ ID NO: 1329 CFFKAIWGLLKSILEGLIDGWYG SEQ ID NO: 1330 CFFKAIWGLLKNIFKGLIDG SEQ ID NO: 1331 CFFKAIWGLLKNIFKGLIDGWYG SEQ ID NO: 1332 CFFKAIWGLLKNIFEGLIDG SEQ ID NO: 1333 CFFKAIWGLLKNIFEGLIDGWYG SEQ ID NO: 1334 CFFKAIWEFIKSILKGLIDGWNG SEQ ID NO: 1335 CFFKAIWEFIKNIFKGLIDGWNG SEQ ID NO: 1336 CIFGAIAGLLKNILKGLIDG SEQ ID NO: 1337 CIFGAIAGLLKNILKGLIDGWYG SEQ ID NO: 1338 CFLEALWKALEHLL SEQ ID NO: 1339 CFLEALWEALSKLL SEQ ID NO: 1340 CFLEALWEALEKLL SEQ ID NO: 1341 CFLEALWEALEHLLK(stearyl) SEQ ID NO: 1342 (stearyl)FLEALWEALEHLLC SEQ ID NO: 1343 (stearyl)GFLEALWEALEHLLC SEQ ID NO: 1344 CFLEALWKALSKLL SEQ ID NO: 1345 CFLEALWEALDHLL SEQ ID NO: 1346 CFLEALWEALTHLL SEQ ID NO: 1347 CFLEALWEALNHLL SEQ ID NO: 1348 CFLEALWEALQHLL SEQ ID NO: 1349 CFLEALWEALEHLLH SEQ ID NO: 1350 CFLEALWEALEHLLK SEQ ID NO: 1351 CFLEALWEALEHLLE SEQ ID NO: 1352 CWLEALEALEHLL SEQ ID NO: 1353 CLLEALWEALEHLL SEQ ID NO: 1354 CFFEALWEALEHLL SEQ ID NO: 1355 CFLEALEEALEHLL SEQ ID NO: 1356 CFLEALAEALEHLL SEQ ID NO: 1357 CFLEALFEALEHLL SEQ ID NO: 1358 CLFEALWEALHHLL SEQ ID NO: 1359 CLFEALWEALKHLL SEQ ID NO: 1360 CFLEALWEALEHGL SEQ ID NO: 1361 CLFEALWEALEHLF SEQ ID NO: 1362 CLFEALWEALEHFL SEQ ID NO: 1363 CLFEALWEALEHLLEGLIDWWYG SEQ ID NO: 1364 CLFEALWEALEHLLEGLIDWWNG SEQ ID NO: 1365 CLFEALWEALEHLLENLIDWWNG SEQ ID NO: 1366 CFLEELWELLEKLL SEQ ID NO: 1367 CFLEELWELLEELLE SEQ ID NO: 1368 CFLEELWELLEELLELLE SEQ ID NO: 1369 CFLEELWELLEHLLELLD SEQ ID NO: 1370 CFLEELWELLEELLELID SEQ ID NO: 1371 CFLEELWELLEELLELLD SEQ ID NO: 1372 CFLEELWELLEHLLEGLE SEQ ID NO: 1373 CFLEELWELLEHLLEGLD SEQ ID NO: 1374 CFLEELWELLEHLLEEGLI SEQ ID NO: 1375 CFLEELWELLEHLLEGLIDWWYG SEQ ID NO: 1376 CFLEELWELLEHLLENLIDWWNG SEQ ID NO: 1377 CFLEALWEALEHLLELLD SEQ ID NO: 1378 CGLFGELEELLEEGLENLTDWWNG SEQ ID NO: 1379 CGLFGELEELLEEGLENL-(ALLO-I)-DWWNG SEQ ID NO: 1380 CFLEALWEALEHLLELID SEQ ID NO: 1381 CELFEELEELLEEGLENLIDWWNG SEQ ID NO: 1382 CGLFEELEELLEEGLELLIDWWNG SEQ ID NO: 1383 CGLFEELEELLEEGLELLIDWWNK SEQ ID NO: 1384 CGLFEELEELLEEGLENLIDWWNK SEQ ID NO: 1385 CGLFGELEELLEEGLENLIDWWNQ SEQ ID NO: 1386 CGLFGELEELLEEGLENLIDWWNE SEQ ID NO: 1387 CGLFGELEELLEEGLENLIDWWNN SEQ ID NO: 1388 CGLFGELEELLEEGLENLIDWWNS SEQ ID NO: 1389 CGLFEELEELLEEGLENLIDWWNQ SEQ ID NO: 1390 AC-CFLEELWELLEHLL SEQ ID NO: 1391 AC-CFLEELWELLEELL SEQ ID NO: 1392 CGLLGEIEELLEEGLENLIDWWNG SEQ ID NO: 1393 CGLLAEIEELLEEGLENLIDWWNG SEQ ID NO: 1394 CGLLGEIEELLEEGLENLIDWWNQ SEQ ID NO: 1395 CGLLAEIEELLEEGLENLIDWWNQ SEQ ID NO: 1396 CGLLEEIEELLEEGLENLIDWWNQ SEQ ID NO: 1397 CGLLGEIEELLEEGLENLIDWWNE SEQ ID NO: 1398 CGLLAEIEELLEEGLENLIDWWNE SEQ ID NO: 1399 CGLLEEIEELLEEGLENLIDWWNE SEQ ID NO: 1400 CGLLGEIEELLEEGLENLIDWWNS SEQ ID NO: 1401 CGLLAEIEELLEEGLENLIDWWNS SEQ ID NO: 1402 CGLLEEIEELLEEGLENLIDWWNS SEQ ID NO: 1403 CGLFAELEELLEEGLENLLEWWNG SEQ ID NO: 1404 CGLFEELEELLEEGLENLLEWWNG SEQ ID NO: 1405 CGLFGELEELLEEGLENLLEWWNE SEQ ID NO: 1406 CGLFAELEELLEEGLENLLEWWNE SEQ ID NO: 1407 CGLFEELEELLEEGLENLLEWWNE SEQ ID NO: 1408 CGLLGELEELLEEGLENLLEWWNG SEQ ID NO: 1409 CGLLGELEELLEEGLENLLEWWNE SEQ ID NO: 1410 CGILGEIEELLEEGLENLIDWWNG SEQ ID NO: 1411 CGILGEIEELLEEGLENLIDWWNE SEQ ID NO: 1412 CGILGEIEELLEEGLENLIDWWNS SEQ ID NO: 1413 CGILAEIEELLEEGLENLIDWWNG SEQ ID NO: 1414 CGILEEIEELLEEGLENLIDWWNG SEQ ID NO: 1415 CIFGAIAELLKNIFK SEQ ID NO: 1416 CIFGAIAELLENIFK SEQ ID NO: 1417 CIFGAIAGLLENIFK SEQ ID NO: 1418 CFLEELWGLLEHLL SEQ ID NO: 1419 CGILAEIEELLEEGLENLIDWWNQ SEQ ID NO: 1420 CGILAEIEELLEEGLENLIDWWNE SEQ ID NO: 1421 CGLFAEIEELLEEGLENLIDWWNQ SEQ ID NO: 1422 CGLFAEIEELLEEGLENLIDWWNE SEQ ID NO: 1423 CGLFGELEELLEEGLENLLEWWNQ SEQ ID NO: 1424 CGLFAEIAELLEEGLE-CIT-LIDWWNE SEQ ID NO: 1425 CGILAEIEELLEEGLENLLEWWNG SEQ ID NO: 1426 CGILEEIEELLEEGLENLIDWWNE SEQ ID NO: 1427 CGILEEIEELLEEGLENLIDWWNQ SEQ ID NO: 1428 CGLFGEIEELIWEGLENLIDWWNG SEQ ID NO: 1429 CGLFGEIAELIWEGLENLIDWWNG SEQ ID NO: 1430 CGLFEEIAELIEEGLENLIDWWNG SEQ ID NO: 1431 CGLFEEIAELIWEGLENLIDWWNG SEQ ID NO: 1432 CELFEEIAELIWEGLENLIDWWNG SEQ ID NO: 1433 CELFEEIAELLWEGLENLIDWWNG SEQ ID NO: 1434 CGLFEEIAELLWEGLENLIDWWNG SEQ ID NO: 1435 CGLFEELAELLWEGLENLIDWWNG SEQ ID NO: 1436 CELFEELAELLWEGLENLIDWWNG SEQ ID NO: 1437 CELFEELAELLWEGLENLIDWWNS SEQ ID NO: 1438 CGLFEELAELLWEGLENLIDWWNS SEQ ID NO: 1439 CGIFEELAELLWEGLENLIDWWNG SEQ ID NO: 1440 CGIFEELAELLWEGLENLIDWWNS SEQ ID NO: 1441 CGLFEELEELLEELLENLIDWWNS SEQ ID NO: 1442 CELFEELEELLEELLENLIDWWNS SEQ ID NO: 1443 CELFEELEELLEELLELLIDWWNS SEQ ID NO: 1444 CEFLEELEELLEELLENLIDWWNS SEQ ID NO: 1445 CELFEELEELLEHLLENLIDWWNS SEQ ID NO: 1446 CELFEELEELLHELLENLIDWWNS SEQ ID NO: 1447 CGLFGELEELLWEGLENLIDWWNG SEQ ID NO: 1448 CGLFGELEELLWEGLHNLIDWWNG SEQ ID NO: 1449 CGLFGELWELLEHGLENLIDWWNG SEQ ID NO: 1450 CGL-R6H-GELEEL-S7H-EEGLENLIDWWNG SEQ ID NO: 1451 CGLFEAIEGFIENGWEGMIDGWNG SEQ ID NO: 1452 CGLFEAIEGFIENGWEGMIDWWNG SEQ ID NO: 1453 CGLFGAIEGFIENGWEGMIDWWNG SEQ ID NO: 1454 CGLFAEIEELLEEGLENLLEWWNG SEQ ID NO: 1455 CGLFAELEELLEEGLENLIDWWNG SEQ ID NO: 1456 CGIFAEIEELLEEGLENLIDWWNG SEQ ID NO: 1457 CGLFAEIEELLEEGLENLIDWWNGF SEQ ID NO: 1458 CGLFAEIEELLEEGLENLIDWWNA SEQ ID NO: 1459 CGLFAEIEELLEEGLENLIDWWNS SEQ ID NO: 1460 CGLFAEIEELLEEGLENLIDWWN-CIT SEQ ID NO: 1461 CGLFGEIAGLLEEGLHNLIDWWNG SEQ ID NO: 1462 CGLFGEIAGLLEQGLHNLIDWWNG SEQ ID NO: 1463 CGLFGEIAGLLESGLHNLIDWWNG SEQ ID NO: 1464 CGLFAEIAGLLEQGLHNLIDWWNG SEQ ID NO: 1465 CGLFAEIAGLLEEGLHNLIDWWNG SEQ ID NO: 1466 CGLFAEIAGLLESGLHNLIDWWNG SEQ ID NO: 1467 CGIFEAIAGLLEQGLHNLIDWWNG SEQ ID NO: 1468 CGLFGAIAELLEEGLHNLIDWWNG SEQ ID NO: 1469 CGLFAAIAELLEEGLHNLIDWWNG SEQ ID NO: 1470 CGIFEAIAGLLKNIFKNLIDWWNG SEQ ID NO: 1471 CGIFGAIWELLEQGLHNLIDWWNG SEQ ID NO: 1472 CGLFAELAGLLEQGLHNLIDWWNG SEQ ID NO: 1473 CGILAELAGLLEQGLHNLIDWWNG SEQ ID NO: 1474 CGLFGEIEELLEHLL SEQ ID NO: 1475 CGLFGEIEELLEELL SEQ ID NO: 1476 CGLFGEIEELLEEGL SEQ ID NO: 1477 CGLFGEIEELLEHGL SEQ ID NO: 1478 CGLFHEIEELLEHLL SEQ ID NO: 1479 CFLGALWKALSELLE SEQ ID NO: 1480 CGLFGEIWELLEEGL SEQ ID NO: 1481 CGLFGEIWELLEEGLI SEQ ID NO: 1482 CGLFGEIWELLEELL SEQ ID NO: 1483 CGLFEEIEELLEELLE SEQ ID NO: 1484 CGLFELIEGFIEWGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 1485 CIFGAIAGFIKNIWLHLLHHLLHHLHHLLHHLLHL SEQ ID NO: 1486 CEALFGKINAIFIGKL SEQ ID NO: 1487 CEENWIGLFGGGNIWEEEEILDLL SEQ ID NO: 1488 CLELWLEHLFLELE SEQ ID NO: 1489 CGNFEEIEGFIENGWEGLIDGWYGYGRKKRRQRR SEQ ID NO: 1490 CRGKWYMGFGEIKRQGEGRRYGLFEDWIAENRGI SEQ ID NO: 1491 GLFEAIEGFIENGWEGLAELAEALEALAAGGSC SEQ ID NO: 1492 GLFGALAEALAEALAEHLAEALAEALEALAAGGSC SEQ ID NO: 1493 CGFFGEIAGLLENGLHNLIDWWNG SEQ ID NO: 1494 CGFFGEIAALLENGLENLIDWWNG SEQ ID NO: 1495 CGFFGEIAEFIHSGLKNLIDWWNG SEQ ID NO: 1496 CGFFGEIAGLLKNGLKNLIDWWNG SEQ ID NO: 1497 CGFFGEIAGFIKNGLKNLIDWWNG SEQ ID NO: 1498 CGFFGEIAEFIHSILKNLIDWWNG SEQ ID NO: 1499 CGFFGEIAGLLKNILKNLIDWWNG SEQ ID NO: 1500 CGFFGEIAGFIKNILKNLIDWWNG SEQ ID NO: 1501 CFLGALFHALSELL SEQ ID NO: 1502 CFLGALWHALSELL SEQ ID NO: 1503 CFLGALWHALSHLL SEQ ID NO: 1504 CFLGALWELLSHLL SEQ ID NO: 1505 CFLGALWKALSHLL SEQ ID NO: 1506 CFLGALWHALSKLL SEQ ID NO: 1507 CFLGALFHLLSHLL SEQ ID NO: 1508 CFLGALFHLLSELL SEQ ID NO: 1509 CFLGALWHLLSHLL SEQ ID NO: 1510 CFLGALWHLLSELL SEQ ID NO: 1511 CFLGALFHALSHLLE SEQ ID NO: 1512 CFLGALFHLLSHLLE SEQ ID NO: 1513 CGLFGALFHALSHLLE SEQ ID NO: 1514 CFLGALWKALSHLL SEQ ID NO: 1515 CGLFAEIEELLEEGLENLIDWWNG SEQ ID NO: 1516 CGLFGEIEELIEEGLE-Cit-LIDWWNG SEQ ID NO: 1517 CGLFGEIEELIEEGLENLIDWWNE SEQ ID NO: 1518 CFFGAIWEFIHSILK(stearyl) SEQ ID NO: 1519 CIFGAIAGFIKNIWEGLIK(stearyl) SEQ ID NO: 1520 CGIFEAIAGLLKNIFK(stearyl) SEQ ID NO: 1521 CGIFEAIAGLLKNIFKK(stearyl) SEQ ID NO: 1522 CFLGALFHALSHLL SEQ ID NO: 1523 Ac-CIFGAIAGFIKNILKGLIDG SEQ ID NO: 1524 CIFGAIAGFIKNILKGLK(stearylL) SEQ ID NO: 1525 Ac-CIFGAIAGFIKNILKGLK(stearyl) SEQ ID NO: 1526 CGLFGEIEELIEEGLENLIDWWNG SEQ ID NO: 1527 CFLGALWKALSELLKNLIDWWNG SEQ ID NO: 1528 CGFLGALWKALSELLKNLIDWWNG SEQ ID NO: 1529 CFLGALFHALSHLLENLIDWWNG SEQ ID NO: 1530 CGFLGALFHALSHLLENLIDWWNG SEQ ID NO: 1531 CGLFGELEGFIENGLKNLIDWWNG SEQ ID NO: 1532 CGLFGELEGLLWHGLKNLIDWWNG SEQ ID NO: 1533 CGLFGELAELLWHGLKNLIDWWNG SEQ ID NO: 1534 CGLFGELAELLWQGLKNLIDWWNG SEQ ID NO: 1535 CGLFGELWELLWHGLKNLIDWWNG SEQ ID NO: 1536 CGLFGELWELLWQGLKNLIDWWNG SEQ ID NO: 1537 CGLFEELAGLLWHGLKNLIDWWNG SEQ ID NO: 1538 CGLFEELWGLLWHGLKNLIDWWNG SEQ ID NO: 1539 CGLFEELAGLLWQGLKNLIDWWNG SEQ ID NO: 1540 CGLFEELWGLLWQGLKNLIDWWNG SEQ ID NO: 1541 CGLFGELAELLWHGLKNLIDWWNK SEQ ID NO: 1542 CGLFEELAELLWHGLKNLIDWWNK SEQ ID NO: 1543 CGLFGELAELLWHGLKNLIDWWNH SEQ ID NO: 1544 CGLFEELAELLWHGLKNLIDWWNH SEQ ID NO: 1545 CGLFAELWGLLWQGLKNLIDWWNG SEQ ID NO: 1546 CGLFAELWGLLWHGLKNLIDWWNG SEQ ID NO: 1547 CGLFAELWGLLWHGLHNLLDWWNG SEQ ID NO: 1548 CGLFAELAELLWEGLKNLIDWWNG SEQ ID NO: 1549 CGLFAELAELLWHGLKNLIDWWNG SEQ ID NO: 1550 CGLFAELELLWQGLKNLIDWWNG SEQ ID NO: 1551 CELFGELAGLLWHGLKNLIDWWNG SEQ ID NO: 1552 CLFEALWE-Aib-LEKLF SEQ ID NO: 1553 CFLEALWELLEHLL SEQ ID NO: 1554 CFLEALWKALEKLL SEQ ID NO: 1555 CGLF-Aib-EIAGLLEEGLHNLIDWWNG SEQ ID NO: 1556 CGLFGEI-Aib-GLLEEGLHNLIDWWNG SEQ ID NO: 1557 CGFFGEIAGLLEE-Aib-LHNLIDWWNG SEQ ID NO: 1558 CGLFGEIAGLLEEGLHNLIDWWN-Aib SEQ ID NO: 1559 CGLF-Aib-EIAGLLEE-Aib-LHNLIDWWNG SEQ ID NO: 1560 CGFFGEI-Aib-GLLEE-Aib-LHNLIDWWNG SEQ ID NO: 1561 CGFFGEI-Aib-ELIWEGLKNLIDWWNG SEQ ID NO: 1562 CGFFGEIAELIWELKNLIDWWN-Aib SEQ ID NO: 1563 CGFF Aib-EIAELIWE-Aib-LKNLIDWWNG SEQ ID NO: 1564 AC-CFLGALWKALSHLL SEQ ID NO: 1565 AC-CFLEELWELLEELLE SEQ ID NO: 1566 AC-CLFGALWKALSELL SEQ ID NO: 1567 AC-CGIGAVLKVLTTGLPALISWIKRKRQQ SEQ ID NO: 1568 AC-CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 1569 AC-CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRRK(stearyl) SEQ ID NO: 1570 Ac-CFLGALWKALSHLL SEQ ID NO: 1571 Ac-CFLGALWKALSELL SEQ ID NO: 1572 CELFEEIAELLWEGLENLIDWWNG SEQ ID NO: 1573 CGLFGEIAELIWEGLENLIDWWNG SEQ ID NO: 1574 CGLFGEIEELLEEGLENLIDWWNG SEQ ID NO: 1575 CGLFAELAELLWEGLENLIDWWNG SEQ ID NO: 1576 CGLFAELAELLEEGLENLIDWWNG SEQ ID NO: 1577 CGLFAELAELLWEGLENLIDWWNS SEQ ID NO: 1578 CGLFAELAELLEEGLENLIDWWNS SEQ ID NO: 1579 CGLFAELAELLWEGLENLIDWWNQ SEQ ID NO: 1580 CGLFAELAELLEEGLENLIDWWNQ SEQ ID NO: 1581 CGLFAELAELLWEGLENLIDWWNE SEQ ID NO: 1582 CGLFAELAELLEEGLENLIDWWNE SEQ ID NO: 1583 CELFEELAELLWEGLENLIDWWNQ SEQ ID NO: 1584 CELFEELAELLWEGLENLIDWWNE SEQ ID NO: 1585 CELFEELAELLEEGLENLIDWWNG SEQ ID NO: 1586 CELFAELAELLWEGLENLIDWWNG SEQ ID NO: 1587 CELFAELAELLEEGLENLIDWWNG SEQ ID NO: 1588 CELFAELAELLWEGLENLIDWWNS SEQ ID NO: 1589 CELFAELAELLEEGLENLIDWWNS SEQ ID NO: 1590 CELFAELAELLWEGLENLIDWWNQ SEQ ID NO: 1591 CELFAELAELLEEGLENLIDWWNQ SEQ ID NO: 1592 CELFAELAELLWEGLENLIDWWNE SEQ ID NO: 1593 CELFAELAELLEEGLENLIDWWNE SEQ ID NO: 1594 CELFEELAELLWEGLHNLIDWWNG SEQ ID NO: 1595 CELFEELAELLWEGLHNLIDWWNS SEQ ID NO: 1596 CELFEELAELLWEGLHNLIDWWNQ SEQ ID NO: 1597 CELFEELAELLWEGLHNLIDWWNE SEQ ID NO: 1598 CELFGELEGFIENGLENLIDWWNG SEQ ID NO: 1599 CGLFEELEGFIENGLENLIDWWNG SEQ ID NO: 1600 CGLFAELAGFIENGLENLIDWWNG SEQ ID NO: 1601 CGLFAELEGFIENGLENLIDWWNG SEQ ID NO: 1602 CGLFGELAGFIENGLENLIDWWNG SEQ ID NO: 1603 CELFEELEGFIENGLENLIDWWNG SEQ ID NO: 1604 CELFAELAGFIENGLENLIDWWNG SEQ ID NO: 1605 CGLFGELEGFIWNGLENLIDWWNG SEQ ID NO: 1606 CGLFGELEGFIENGLENLIDWWNG SEQ ID NO: 1607 CGLFGELEGFIENGLENLIDWWNQ SEQ ID NO: 1608 CGLFGELEGFIENGLENLIDWWNE SEQ ID NO: 1609 CELFEELEGFIENGLENLIDWWNE SEQ ID NO: 1610 CGLLEEIAELLEEGLENLIDWWNS SEQ ID NO: 1611 CGLLEEIEELLWEGLENLIDWWNS SEQ ID NO: 1612 CELLEEIEELLEEGLENLIDWWNS SEQ ID NO: 1613 CGLLEEIAELLWEGLENLIDWWNS SEQ ID NO: 1614 CELLEEIAELLWEGLENLIDWWNS SEQ ID NO: 1615 CELLEEIEELLEEGLENLIDWWNE SEQ ID NO: 1616 CGLLEELEELLEEGLENLIDWWNS SEQ ID NO: 1617 CGLLEELEELLEEGLENLLEWWNS SEQ ID NO: 1618 CGLLEEIAELLEEGLENLIDWWNG SEQ ID NO: 1619 CGLLAEIAELLEEGLENLIDWWNS SEQ ID NO: 1620 CGLLAEIAELLWEGLENLIDWWNS SEQ ID NO: 1621 CGLLEEIEGFIENGLENLIDWWNS SEQ ID NO: 1622 CGLLEEIEGFIENGLENLIDWWNG SEQ ID NO: 1623 CGLLEEIEELLEEGLE-Cit-LIDWWNS SEQ ID NO: 1624 CGLLEEIEELLEQGLENLIDWWNS SEQ ID NO: 1625 CGLLAELAELLEEGLENLIDWWNS SEQ ID NO: 1626 CGLLEEIEELLEEGLENLIDWWNA SEQ ID NO: 1627 CGLL-Aib-EIEELLEEGLENLIDWWNS SEQ ID NO: 1628 CGLLEEIEELLEEGLENLIDWWN-Aib SEQ ID NO: 1629 CGLLEEIEELLEE-Aib-LENLIDWWNG SEQ ID NO: 1630 CGLFGHIHHLIHHGLHNLIDWWNG SEQ ID NO: 1631 CGLFGEIHHLIHHGLHNLIDWWNG SEQ ID NO: 1632 CGLFGEIHHLIHHGLENLIDWWNG SEQ ID NO: 1633 CGLFGEIHELIHHGLENLIDWWNG SEQ ID NO: 1634 CELLEEIEELLEEGLENLIDWWNS SEQ ID NO: 1635 CGLFGELEELIEEGLENLIDWWNG SEQ ID NO: 1636 CGLLAEIEELLWEGLENLIDWWNS SEQ ID NO: 1637 CGLLEEIEELLEEGLENLLEWWNS SEQ ID NO: 1638 C(b-ALA)LLEEIEELLEEGLENLIDWWNS SEQ ID NO: 1639 CGLLEEIEELLEEGLENLIDLWNS SEQ ID NO: 1640 CGLLEEIEELLEWGLENLIDWWNS SEQ ID NO: 1641 CGLFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1642 CGFFGEIAELIEEGLKNLIDWGNG SEQ ID NO: 1643 CGLFGEIEELIEEGLENLIDWANG SEQ ID NO: 1644 CGLFGEIEELIEEGLENLIDWSNG SEQ ID NO: 1645 CGLFGEIEELIEEGLENLIDW-(Aib)-NG SEQ ID NO: 1646 CGLFGEIEELIEEGLENLIDWPNG SEQ ID NO: 1647 CGLFGEIEELIEEGLENLIDWHNG SEQ ID NO: 1648 CGLFGEIEELIEEGLENLIDWQNG SEQ ID NO: 1649 CGLFGEIEELIEEGLENLIDWENG SEQ ID NO: 1650 CGLFEEIAELIEEGLENLIDWGNG SEQ ID NO: 1651 CELFEELAELLWEGLENLIDWGNS SEQ ID NO: 1652 CGLFGEIAELIWEGLENLIDWGNG SEQ ID NO: 1653 CGLLEEIEELLEEGLENLIDWGNS SEQ ID NO: 1654 CGLFAEIEELLEEGLENLIDWGNG SEQ ID NO: 1655 CGLL-(Aib)-EIEELLEEGLENLIDWWNS SEQ ID NO: 1656 CGLFGEIEELIEEGLENLIDWNNG SEQ ID NO: 1657 CGLFGEIEELIEEGLENLIDWDNG SEQ ID NO: 1658 CGLFGEIEELIEEGLENLIDWONG SEQ ID NO: 1659 CGLFAEIEELLEEGLENLIDWGNG SEQ ID NO: 1660 CGLL-Aib-EIEELLEEGLENLIDWGNS SEQ ID NO: 1661 CGLFGEIEELIEEGLENLIDGWNG SEQ ID NO: 1662 CGLFGEIEELIEEGLENLIDLWNG SEQ ID NO: 1663 CGWFGEIEELIEEGLENLIDWWNG SEQ ID NO: 1664 CGLFGEVEELIEEGLENLIDWWNG SEQ ID NO: 1665 CGLFGEIEEVIEEGLENLIDWWNG SEQ ID NO: 1666 CGLFGEIEELVEEGLENLIDWWNG SEQ ID NO: 1667 CGLFGEIEELAEEGLENLIDWWNG SEQ ID NO: 1668 CGLFGEIEELIDEGLENLIDWWNG SEQ ID NO: 1669 CGLFGEIEELIEDGLENLIDWWNG SEQ ID NO: 1670 CGLFGEIEELIEEGLEALIDWWNG SEQ ID NO: 1671 CGLFGEIEELIEEGLENIIDWWNG SEQ ID NO: 1672 CGLFGEIEELIEEGLEN-(Nle)-IDWWNG SEQ ID NO: 1673 CGLFGEIEELIEEGLENLIGWWNG SEQ ID NO: 1674 CGLFELIEGFIENGWEGMIDGWYGYGRKKRRQRR all (D) SEQ ID NO: 1675 CGLFEAIEGFIENGWEGMIDGWYG all (D) SEQ ID NO: 1676 CGLFGEIEELIENGLKNLIDWWYGYGRKKRRQRR all (D) SEQ ID NO: 1677 CGLFEALLELLESLWELLLEAYGRKKRRQRR all (D) SEQ ID NO: 1678 CGLFEEIEGFIENGWEGLIDWWYGYGHKKHHQHR all (D) SEQ ID NO: 1679 CGLFGEIEELIEEGLENLIDWWNE all (D) SEQ ID NO: 1680 CGLFGEIEELIEEGLENLIDWWNS all (D) SEQ ID NO: 1681 CGLFGEIEELIEEGLENLIDWWNQ all (D) SEQ ID NO: 1682 CYGRKKRRQRRLIRLWSHLIHIWFQNRRLKWKKK SEQ ID NO: 1683 CGLFEAIEEFIENGWEGMIDGWYGYGRKKRRQRR SEQ ID NO: 1684 CGLFFAIEGFIENGWEGMIDWWYGYGRKKRRQRR ALL (D) SEQ ID NO: 1685 CGLFELIEGFIENGWEGMIDGWYGYGRKKRRQRRK(STEARYL) ALL (D) SEQ ID NO: 1686 (STEARYL)GLFELIEGFIENGWEGMIDGWYGYGRKKRRQRRC ALL (D) SEQ ID NO: 1687 CFFGAIWEFIKSILK(STEARYL) +C-TERM K(STEARYL) ALL(D) SEQ ID NO: 1688 CFFGAIWEFIKSILK(STEARYL) +C-TERM K(STEARYL) ALL(D) SEQ ID NO: 1689 LAURYL-FFGAIWEFIKSILC ALL (D) SEQ ID NO: 1690 CFFGAIWEFIHSILK(STEARYL) ALL (D) SEQ ID NO: 1691 CGFFGEIAELIEEGLKNLIDWWNG ALL (D) SEQ ID NO: 1692 CGIFEAIAGLLKNIFKGIFEAIAGLLKNIFK ALL (D) SEQ ID NO: 1693 CIFGAIAGFIKNILKGLIDG ALL (D) SEQ ID NO: 1694 CGLFEAIEGFIENGWEGMIDGWYGYGRKKRRQRRK(stearyl) all(D) SEQ ID NO: 1695 (LAURYL)FFGAIWEFIKSILC all (D) SEQ ID NO: 1696 CGLFGEIEELIEEGLENLIDWDNG SEQ ID NO: 1696 glfgeieeliecglenlidwgng SEQ ID NO: 1697 glfgeieelieeclenlidwgng SEQ ID NO: 1698 cglfgeeleelleeglenlidg SEQ ID NO: 1699 cglfgeeleelleeglenlieg SEQ ID NO: 1700 CGLFGEIEELIEEGLENLIDW-Aib-NG SEQ ID NO: 1701 AC-GLLEEIEELLEEGLENLIDWWNSC SEQ ID NO: 1702 GLLEEIEELLEEGLENLAELAEALEALAAGGSC SEQ ID NO: 1703 CGLFGEIEELIEEGLENLIDW SEQ ID NO: 1704 CGLFGEIEELIEEGLENLID SEQ ID NO: 1705 CGLFGEIEELIEEGLENLI SEQ ID NO: 1706 CELFEEIAELIEEGLENLIDWG SEQ ID NO: 1707 AC-GLFGEIEELIEEGLENLIDWGNGC SEQ ID NO: 1708 AC-CGLFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1709 AC-CGLFGEIEELIEEGLENLIDWWNG SEQ ID NO: 1710 CGFFGEI-AIB-GLLEE-AIB-LHNLIDWWNG SEQ ID NO: 1711 CFLGALWKALSELLKNLIDWWNG SEQ ID NO: 1712 CGL-R6H-GELEEL-S7H-EEGLENLIDWWNG (STAPLED) SEQ ID NO: 1713 CGL-R6H-GELEEL-S7H-EEGLENLIDWWNG (STAPLED) SEQ ID NO: 1714 CGFFGEI-AIB-ELIWE-AIB-LKNLIDWWNG SEQ ID NO: 1715 CGLFEELAGLLWHGLKNLIDWWNG SEQ ID NO: 1716 CFLGALFHALSHLLENLIDWWNG SEQ ID NO: 1717 CGFF-AIB-EIAELIWE-AIB-LKNLIDWWNG SEQ ID NO: 1718 CGLFAEIEELIWEGLENLIDWWNQ SEQ ID NO: 1719 STEARYL-AGYLLGKLL-ORN-ORN-LAAAAL-ORN-ORN-LLC SEQ ID NO: 1720 R-AHX-R-AHX-RILFQYR-AHX-B_ALA-R-AHX-R-B_ALA-C SEQ ID NO: 1721 R-AHX-RR-BALA-R-AHX-EIFFQYR-AHX-R-BALA-R-AHX-R- SEQ ID NO: 1722 B_ALA-C R-AHX-RR-BALA-RR-AHX-RILFQYR-AHX-R-B_ALA-R-AHX-R- SEQ ID NO: 1723 B_ALA-C R-AHX-RR-AHX-RR-AHX-RIHILFQNRRMKWHK-B_ALA-C SEQ ID NO: 1724 CSSAWWSYWPPVA SEQ ID NO: 1725 CGLFAVIKKVASVIGGL SEQ ID NO: 1726 CGLFAVIHHVASVIGGL SEQ ID NO: 1727 CGLFAVIEEVASVIGGL SEQ ID NO: 1728 CGPSQPTYPGDDAPVRDLIRFYRDLRRYLNVVTRHRY SEQ ID NO: 1729 CGIGAVLHVLTTGLPALISWIKRKRQQ SEQ ID NO: 1730 CGIGAVLHVLTTGLPALISWIHHHHQQ SEQ ID NO: 1731 AC-GIFEAIAGLLKINFKC SEQ ID NO: 1732 AC-GLFGALAEALAEALAEHLAEALAEALEALAAGGSC SEQ ID NO: 1733 AC-GLFEAIEGFIENGWEGLAELAEALEALAAGGSC SEQ ID NO: 1734 AC-GIFEAIAGLLKINFKC SEQ ID NO: 1735 AC-GLFGALAEALAEALAEHLAEALAEALEALAAGGSC SEQ ID NO: 1736 AC-GLFGALAEALAEALAEHLAEALAEALEALAAGGSC SEQ ID NO: 1737 GLFGEIEELIEEGLENLIDWGNGLAELAEALEALAAGGSC SEQ ID NO: 1738 GLFGEIEELIEEGLENLIDWGNGLAELAEALEALAAGGSC SEQ ID NO: 1739 GLFEAIEGFIENGWEGLAELAEALEALAAGGSC SEQ ID NO: 1740 GLFGALAEALAEALAEHLAEALAEALEALAAGGSC SEQ ID NO: 1741 GLFEAIEGFIENGWEGLAELAEALEALAAGGSC SEQ ID NO: 1742 GLFEAIEGFIENGWEGLAELAEALEALAAGGSC SEQ ID NO: 1743 CEENWIGLFGGGNIWEEEEILDLL SEQ ID NO: 1744 CGLFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1745 CEALFGKINAIFIGKL SEQ ID NO: 1746 CGLFGEIEELLEEGLENLIDWGNG SEQ ID NO: 1747 CGLFGEIEELIEEALENLIDWGNG SEQ ID NO: 1748 CGLFGEIEELIEEGFENLIDWGNG SEQ ID NO: 1749 CGLFGEIEELIEEGFENLIDWGNG SEQ ID NO: 1750 CGLFGEIEELIEEGWENLIDWGNG SEQ ID NO: 1751 CGLFGEIEEWIEEGLENLIDWGNG SEQ ID NO: 1752 CGLFGEIEEFIEEGLENLIDWGNG SEQ ID NO: 1753 CGLFGEIEEFIEEGLENLIDWGNG SEQ ID NO: 1754 CGLFGEIEELFEEGLENLIDWGNG SEQ ID NO: 1755 CGLFGEIEELIEEGLENLIDWGNE SEQ ID NO: 1756 CGLFGEIEELIEEGLENLIDWGNE SEQ ID NO: 1757 CGLFGEIEELIEEGLEELIDWGNG SEQ ID NO: 1758 CGLFGEIEELIEEGLESLIDWGNG SEQ ID NO: 1759 CGLFGEIEELIEEGLEQLIDWGNG SEQ ID NO: 1760 CGLFGEIEELIEEGLENWIDWGNG SEQ ID NO: 1761 CGLFGEIEELIEEGLENFIDWGNG SEQ ID NO: 1762 CGLFGEIEELIEEGLENLWDWGNG SEQ ID NO: 1763 CGLFGEIEELIEEGLENLVDWGNG SEQ ID NO: 1764 CGLFGEIEELIEEGLENLIEWGNG SEQ ID NO: 1765 CGLFGEIEELIEEGLENLIDFGNG SEQ ID NO: 1766 CGLFGEIEELIEEGLENLIDLGNG SEQ ID NO: 1767 CGLFGEIEELIEEGLENLIDWGYG SEQ ID NO: 1768 CGLFGEIEELIEEGLENLIDWGSG SEQ ID NO: 1769 CGLFGEIEELIEEGLENLIDWGNQ SEQ ID NO: 1770 CGLFGEIEELIEEGLENLIDWGN-AIB SEQ ID NO: 1771 CGLFEALLELLESLWELLLEAGYG SEQ ID NO: 1772 CGLFGEIEELIEEGLENLIDWGNS SEQ ID NO: 1746 CGLFEAIEGFIENGWEGMIDWGNG SEQ ID NO: 1773 CIFGIDDLEEGLLFVAIVEAGIGGYLLGS SEQ ID NO: 1774 CGLFEALLELLESLWELLLEA SEQ ID NO: 1775 CGLFGEIEELIEEGLENLIDWGNGC SEQ ID NO: 1776 CGNFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1777 CGLFAEIEELIEEGLENLIDWGNG SEQ ID NO: 1778 CGLFEEIEELIEEGLENLIDWGNG SEQ ID NO: 1779 CGLFGEIAELIEEGLENLIDWGNG SEQ ID NO: 1780 CELFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1781 CALFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1782 C-AIB-LFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1783 CGWFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1784 CGLFGELEELIEEGLENLIDWGNG SEQ ID NO: 1785 CGLFGEIEELWEEGLENLIDWGNG SEQ ID NO: 1786 CGLFGEIEELWEEGLENLIDWGNG SEQ ID NO: 1787 CGLFGEIEELIEE-AIB-LENLIDWGNG SEQ ID NO: 1788 CGLFGEIEELIEE-AIB-LENLIDWGNG SEQ ID NO: 1789 CGLFGEIEELIEE-AIB-LENLIDWGNG SEQ ID NO: 1790 CGLFGEIEELIEE-AIB-LENLIDWGNG SEQ ID NO: 1791 CGLFGEIEELIEE-AIB-LENLIDWGNG SEQ ID NO: 1792 CGLLGEIEELIEEGLENLIDWGNG SEQ ID NO: 1793 CGLFGAIEELIEEGLENLIDWGNG SEQ ID NO: 1794 CGFFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1795 CGLWGEIEELIEEGLENLIDWGNG SEQ ID NO: 1796 CGLFGEWEELIEEGLENLIDWGNG SEQ ID NO: 1797 CGLFGEFEELIEEGLENLIDWGNG SEQ ID NO: 1798 CGLFGEIEELIEEGLENLLDWGNG SEQ ID NO: 1799 CGLFGEIEELIEEGLENLIDWGQG SEQ ID NO: 1800 GLFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1801 GFFGAIWEFIHSIL SEQ ID NO: 1802

A subset of the peptides disclosed in Table 2 that can be used in the conjugates herein are listed in Table 2a.

TABLE 2a Suitable Peptide Sequences and ID Peptide Sequence SEQ ID NO: CIFGAIAGFIKNIWEGLI SEQ ID NO: 26 CFFGAIWEFIHSIL SEQ ID NO: 74 CGIFEAIAGLLKNIFK SEQ ID NO: 82 CGIGAVLKVLTTGLPALISWIKRKRQQ SEQ ID NO: 255 CGFFGEIAELIEEGLKNLIDWWNG SEQ ID NO: 543 CGFFGEIAELIWEGLKNLIDWWNG SEQ ID NO: 935 CGLFGEIEELIEEGLENLIDWANG SEQ ID NO: 1078 CFLEELWELLEHLL SEQ ID NO: 1248 AC-CFLEELWELLEHLL SEQ ID NO: 1391 CGLLEEIEELLEEGLENLIDWWNS SEQ ID NO: 1403 CFLEELWGLLEHLL SEQ ID NO: 1419 CLELWLEHLFLELE SEQ ID NO: 1489 CGLFAEIEELLEEGLENLIDWWNG SEQ ID NO: 1516 CGLFGEIEELIEEGLE-CIT-LIDWWNG SEQ ID NO: 1517 CGLFGEIEELIEEGLENLIDWWNE SEQ ID NO: 1518 CGLL-AIB-EIEELLEEGLENLIDWWNS SEQ ID NO: 1628 CGLFGHIHHLIHHGLHNLIDWWNG SEQ ID NO: 1631 CGLFGEIHHLIHHGLHNLIDWWNG SEQ ID NO: 1632 CGLFGEIHHLIHHGLENLIDWWNG SEQ ID NO: 1633 CGLFGEIHELIHHGLENLIDWWNG SEQ ID NO: 1634 CGFFGEIAELIEEGLKNLIDWGNG SEQ ID NO: 1643 CGLFGEIEELIEEGLENLIDWSNG SEQ ID NO: 1645 CGLFGEIEELIEEGLENLIDWPNG SEQ ID NO: 1647 CGLFGEIEELIEEGLENLIDWHNG SEQ ID NO: 1648 CGLFGEIEELIEEGLENLIDWQNG SEQ ID NO: 1649 CGLFGEIEELIEEGLENLIDWENG SEQ ID NO: 1650 CGLFEEIAELIEEGLENLIDWGNG SEQ ID NO: 1651 CELFEELAELLWEGLENLIDWGNS SEQ ID NO: 1652 CGLFGEIAELIWEGLENLIDWGNG SEQ ID NO: 1653 CGLLEEIEELLEEGLENLIDWGNS SEQ ID NO: 1654 CGLFGEIEELIEEGLENLIDWNNG SEQ ID NO: 1657 CGLFAEIEELLEEGLENLIDWGNG SEQ ID NO: 1660 CGLFGEIEELIEEGLENLIDWONG SEQ ID NO: 1662 CGLFGEIEELIEEGLENLIDWDNG SEQ ID NO: 1696 GLFGEIEELIECGLENLIDWGNG SEQ ID NO: 1697 CGLFGEIEELIEEGLENLIDW-AIB-NG SEQ ID NO: 1701 AC-GLLEEIEELLEEGLENLIDWWNSC SEQ ID NO: 1702 GLLEEIEELLEEGLENLAELAEALEALAAGGSC SEQ ID NO: 1703 CGLFGEIEELIEEGLENLIDW SEQ ID NO: 1704 CGLFGEIEELIEEGLENLID SEQ ID NO: 1705 CGLFGEIEELIEEGLENLI SEQ ID NO: 1706 CELFEEIAELIEEGLENLIDWG SEQ ID NO: 1707 AC-GLFGEIEELIEEGLENLIDWGNGC SEQ ID NO: 1708 AC-CGLFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1709 AC-CGLFGEIEELIEEGLENLIDWWNG SEQ ID NO: 1710 CGFFGEI-AIB-GLLEE-AIB-LHNLIDWWNG SEQ ID NO: 1711 CFLGALWKALSELLKNLIDWWNG SEQ ID NO: 1712 CGL-R6H-GELEEL-S7H-EEGLENLIDWWNG (STAPLED) SEQ ID NO: 1713 CGFFGEI-AIB-ELIWE-AIB-LKNLIDWWNG SEQ ID NO: 1715 CGLFEELAGLLWHGLKNLIDWWNG SEQ ID NO: 1716 CFLGALFHALSHLLENLIDWWNG SEQ ID NO: 1717 CGFF-AIB-EIAELIWE-AIB-LKNLIDWWNG SEQ ID NO: 1718 CGLFAEIEELIWEGLENLIDWWNQ SEQ ID NO: 1719 STEARYL-AGYLLGKLL-ORN-ORN-LAAAAL-ORN-ORN-LLC SEQ ID NO: 1720 R-AHX-R-AHX-RILFQYR-AHX-B_ALA-R-AHX-R-B_ALA-C SEQ ID NO: 1721 R-AHX-RR-B_ALA-R-AHX-EIFFQYR-AHX-R-B_ALA-R-AHX-R- SEQ ID NO: 1722 B_ALA-C R-AHX-RR-B_ALA-RR-AHX-RILFQYR-AHX-R-B_ALA-R-AHX-R- SEQ ID NO: 1723 B_ALA-C R-AHX-RR-AHX-RR-AHX-RIHILFQNRRMKWHK-B_ALA-C SEQ ID NO: 1724 CSSAWWSYWPPVA SEQ ID NO: 1725 CGLFAVIKKVASVIGGL SEQ ID NO: 1726 CGLFAVIHHVASVIGGL SEQ ID NO: 1727 CGLFAVIEEVASVIGGL SEQ ID NO: 1728 CGPSQPTYPGDDAPVRDLIRFYRDLRRYLNVVTRHRY SEQ ID NO: 1729 CGIGAVLHVLTTGLPALISWIKRKRQQ SEQ ID NO: 1730 CGIGAVLHVLTTGLPALISWIHHHHQQ SEQ ID NO: 1731 AC-GIFEAIAGLLKINFKC SEQ ID NO: 1732 AC-GLFGALAEALAEALAEHLAEALAEALEALAAGGSC SEQ ID NO: 1733 AC-GLFEAIEGFIENGWEGLAELAEALEALAAGGSC SEQ ID NO: 1734 GLFGEIEELIEEGLENLIDWGNGLAELAEALEALAAGGSC SEQ ID NO: 1738 GLFEAIEGFIENGWEGLAELAEALEALAAGGSC SEQ ID NO: 1740 GLFGALAEALAEALAEHLAEALAEALEALAAGGSC SEQ ID NO: 1741 CEENWIGLFGGGNIWEEEEILDLL SEQ ID NO: 1744 CGLFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1745 CEALFGKINAIFIGKL SEQ ID NO: 1746 CGLFGEIEELLEEGLENLIDWGNG SEQ ID NO: 1747 CGLFGEIEELIEEALENLIDWGNG SEQ ID NO: 1748 CGLFGEIEELIEEGFENLIDWGNG SEQ ID NO: 1749 CGLFGEIEELIEEGWENLIDWGNG SEQ ID NO: 1751 CGLFGEIEEWIEEGLENLIDWGNG SEQ ID NO: 1752 CGLFGEIEEFIEEGLENLIDWGNG SEQ ID NO: 1753 CGLFGEIEELFEEGLENLIDWGNG SEQ ID NO: 1755 CGLFGEIEELIEEGLENLIDWGNE SEQ ID NO: 1756 CGLFGEIEELIEEGLEELIDWGNG SEQ ID NO: 1758 CGLFGEIEELIEEGLESLIDWGNG SEQ ID NO: 1759 CGLFGEIEELIEEGLEQLIDWGNG SEQ ID NO: 1760 CGLFGEIEELIEEGLENWIDWGNG SEQ ID NO: 1761 CGLFGEIEELIEEGLENFIDWGNG SEQ ID NO: 1762 CGLFGEIEELIEEGLENLWDWGNG SEQ ID NO: 1763 CGLFGEIEELIEEGLENLVDWGNG SEQ ID NO: 1764 CGLFGEIEELIEEGLENLIEWGNG SEQ ID NO: 1765 CGLFGEIEELIEEGLENLIDFGNG SEQ ID NO: 1766 CGLFGEIEELIEEGLENLIDLGNG SEQ ID NO: 1767 CGLFGEIEELIEEGLENLIDWGYG SEQ ID NO: 1768 CGLFGEIEELIEEGLENLIDWGSG SEQ ID NO: 1769 CGLFGEIEELIEEGLENLIDWGNQ SEQ ID NO: 1770 CGLFGEIEELIEEGLENLIDWGN-AIB SEQ ID NO: 1771 CGLFEALLELLESLWELLLEAGYG SEQ ID NO: 1772 CGLFEAIEGFIENGWEGMIDWGNG SEQ ID NO: 1773 CIFGIDDLEEGLLFVAIVEAGIGGYLLGS SEQ ID NO: 1774 CGLFEALLELLESLWELLLEA SEQ ID NO: 1775 CGLFGEIEELIEEGLENLIDWGNGC SEQ ID NO: 1776 CGNFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1777 CGLFAEIEELIEEGLENLIDWGNG SEQ ID NO: 1778 CGLFEEIEELIEEGLENLIDWGNG SEQ ID NO: 1779 CGLFGEIAELIEEGLENLIDWGNG SEQ ID NO: 1780 CELFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1781 CALFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1782 C-AIB-LFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1783 CGWFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1784 CGLFGELEELIEEGLENLIDWGNG SEQ ID NO: 1785 CGLFGEIEELWEEGLENLIDWGNG SEQ ID NO: 1786 CGLFGEIEELIEE-AIB-LENLIDWGNG SEQ ID NO: 1788 CGLLGEIEELIEEGLENLIDWGNG SEQ ID NO: 1793 CGLFGAIEELIEEGLENLIDWGNG SEQ ID NO: 1794 CGFFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1795 CGLWGEIEELIEEGLENLIDWGNG SEQ ID NO: 1796 CGLFGEWEELIEEGLENLIDWGNG SEQ ID NO: 1797 CGLFGEFEELIEEGLENLIDWGNG SEQ ID NO: 1798 CGLFGEIEELIEEGLENLLDWGNG SEQ ID NO: 1799 CGLFGEIEELIEEGLENLIDWGQG SEQ ID NO: 1800 GLFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1801 GFFGAIWEFIHSIL SEQ ID NO: 1802

A subset of the peptides disclosed in table 2 that can be used in the conjugates herein are listed in Table 2b.

TABLE 2b Suitable Peptide Sequences and ID Peptide Sequence SEQ ID NO: GLFGEIEELIECGLENLIDWGNG SEQ ID NO: 1697 CGLFGEIEELIEEGLENLIDW-AIB-NG SEQ ID NO: 1701 AC-GLLEEIEELLEEGLENLIDWWNSC SEQ ID NO: 1702 GLLEEIEELLEEGLENLAELAEALEALAAGGSC SEQ ID NO: 1703 CGLFGEIEELIEEGLENLIDW SEQ ID NO: 1704 CGLFGEIEELIEEGLENLID SEQ ID NO: 1705 CGLFGEIEELIEEGLENLI SEQ ID NO: 1706 CELFEEIAELIEEGLENLIDWG SEQ ID NO: 1707 AC-GLFGEIEELIEEGLENLIDWGNGC SEQ ID NO: 1708 AC-CGLFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1709 AC-CGLFGEIEELIEEGLENLIDWWNG SEQ ID NO: 1710 CGFFGEI-AIB-GLLEE-AIB-LHNLIDWWNG SEQ ID NO: 1711 CFLGALWKALSELLKNLIDWWNG SEQ ID NO: 1712 CGL-R6H-GELEEL-S7H-EEGLENLIDWWNG (STAPLED) SEQ ID NO: 1713 CGFFGEI-AIB-ELIWE-AIB-LKNLIDWWNG SEQ ID NO: 1715 CGLFEELAGLLWHGLKNLIDWWNG SEQ ID NO: 1716 CFLGALFHALSHLLENLIDWWNG SEQ ID NO: 1717 CGFF-AIB-EIAELIWE-AIB-LKNLIDWWNG SEQ ID NO: 1718 CGLFAEIEELIWEGLENLIDWWNQ SEQ ID NO: 1719 STEARYL-AGYLLGKLL-ORN-ORN-LAAAAL-ORN-ORN-LLC SEQ ID NO: 1720 R-AHX-R-AHX-RILFQYR-AHX-B_ALA-R-AHX-R-B_ALA-C SEQ ID NO: 1721 R-AHX-RR-B_ALA-R-AHX-EIFFQYR-AHX-R-B_ALA-R-AHX-R- SEQ ID NO: 1722 B_ALA-C R-AHX-RR-B_ALA-RR-AHX-RILFQYR-AHX-R-B_ALA-R-AHX-R- SEQ ID NO: 1723 B_ALA-C R-AHX-RR-AHX-RR-AHX-RIHILFQNRRMKWHK-B_ALA-C SEQ ID NO: 1724 CSSAWWSYWPPVA SEQ ID NO: 1725 CGLFAVIKKVASVIGGL SEQ ID NO: 1726 CGLFAVIHHVASVIGGL SEQ ID NO: 1727 CGLFAVIEEVASVIGGL SEQ ID NO: 1728 CGPSQPTYPGDDAPVRDLIRFYRDLRRYLNVVTRHRY SEQ ID NO: 1729 CGIGAVLHVLTTGLPALISWIKRKRQQ SEQ ID NO: 1730 CGIGAVLHVLTTGLPALISWIHHHHQQ SEQ ID NO: 1731 AC-GIFEAIAGLLKINFKC SEQ ID NO: 1732 AC-GLFGALAEALAEALAEHLAEALAEALEALAAGGSC SEQ ID NO: 1733 AC-GLFEAIEGFIENGWEGLAELAEALEALAAGGSC SEQ ID NO: 1734 GLFGEIEELIEEGLENLIDWGNGLAELAEALEALAAGGSC SEQ ID NO: 1738 GLFEAIEGFIENGWEGLAELAEALEALAAGGSC SEQ ID NO: 1740 GLFGALAEALAEALAEHLAEALAEALEALAAGGSC SEQ ID NO: 1741 CEENWIGLFGGGNIWEEEEILDLL SEQ ID NO: 1744 CGLFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1745 CEALFGKINAIFIGKL SEQ ID NO: 1746 CGLFGEIEELLEEGLENLIDWGNG SEQ ID NO: 1747 CGLFGEIEELIEEALENLIDWGNG SEQ ID NO: 1748 CGLFGEIEELIEEGFENLIDWGNG SEQ ID NO: 1749 CGLFGEIEELIEEGWENLIDWGNG SEQ ID NO: 1751 CGLFGEIEEWIEEGLENLIDWGNG SEQ ID NO: 1752 CGLFGEIEEFIEEGLENLIDWGNG SEQ ID NO: 1753 CGLFGEIEELFEEGLENLIDWGNG SEQ ID NO: 1755 CGLFGEIEELIEEGLENLIDWGNE SEQ ID NO: 1756 CGLFGEIEELIEEGLEELIDWGNG SEQ ID NO: 1758 CGLFGEIEELIEEGLESLIDWGNG SEQ ID NO: 1759 CGLFGEIEELIEEGLEQLIDWGNG SEQ ID NO: 1760 CGLFGEIEELIEEGLENWIDWGNG SEQ ID NO: 1761 CGLFGEIEELIEEGLENFIDWGNG SEQ ID NO: 1762 CGLFGEIEELIEEGLENLWDWGNG SEQ ID NO: 1763 CGLFGEIEELIEEGLENLVDWGNG SEQ ID NO: 1764 CGLFGEIEELIEEGLENLIEWGNG SEQ ID NO: 1765 CGLFGEIEELIEEGLENLIDFGNG SEQ ID NO: 1766 CGLFGEIEELIEEGLENLIDLGNG SEQ ID NO: 1767 CGLFGEIEELIEEGLENLIDWGYG SEQ ID NO: 1768 CGLFGEIEELIEEGLENLIDWGSG SEQ ID NO: 1769 CGLFGEIEELIEEGLENLIDWGNQ SEQ ID NO: 1770 CGLFGEIEELIEEGLENLIDWGN-AIB SEQ ID NO: 1771 CGLFEALLELLESLWELLLEAGYG SEQ ID NO: 1772 CGLFEAIEGFIENGWEGMIDWGNG SEQ ID NO: 1773 CIFGIDDLEEGLLFVAIVEAGIGGYLLGS SEQ ID NO: 1774 CGLFEALLELLESLWELLLEA SEQ ID NO: 1775 CGLFGEIEELIEEGLENLIDWGNGC SEQ ID NO: 1776 CGNFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1777 CGLFAEIEELIEEGLENLIDWGNG SEQ ID NO: 1778 CGLFEEIEELIEEGLENLIDWGNG SEQ ID NO: 1779 CGLFGEIAELIEEGLENLIDWGNG SEQ ID NO: 1780 CELFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1781 CALFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1782 C-AIB-LFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1783 CGWFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1784 CGLFGELEELIEEGLENLIDWGNG SEQ ID NO: 1785 CGLFGEIEELWEEGLENLIDWGNG SEQ ID NO: 1786 CGLFGEIEELIEE-AIB-LENLIDWGNG SEQ ID NO: 1788 CGLLGEIEELIEEGLENLIDWGNG SEQ ID NO: 1793 CGLFGAIEELIEEGLENLIDWGNG SEQ ID NO: 1794 CGFFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1795 CGLWGEIEELIEEGLENLIDWGNG SEQ ID NO: 1796 CGLFGEWEELIEEGLENLIDWGNG SEQ ID NO: 1797 CGLFGEFEELIEEGLENLIDWGNG SEQ ID NO: 1798 CGLFGEIEELIEEGLENLLDWGNG SEQ ID NO: 1799 CGLFGEIEELIEEGLENLIDWGQG SEQ ID NO: 1800 GLFGEIEELIEEGLENLIDWGNG SEQ ID NO: 1801 GFFGAIWEFIHSIL SEQ ID NO: 1802

Linkers

The attachment between a ligand G and an oligonucleotide and/or between a ligand G and a peptide may be mediated by a linker. This linker may be cleavable or non-cleavable, depending on the application. In certain embodiments, a cleavable linker may be used to release the oligonucleotide after transport from the endosome to the cytoplasm. The intended nature of the conjugation or coupling interaction, or the desired biological effect, will determine the choice of linker group. Linker groups may be combined or branched to provide more complex architectures. Suitable linkers include those as described in WO2009/126933, which is hereby incorporated by reference.

In one embodiment, a suitable linker is selected from Table 3:

TABLE 3 Suitable Linkers

Note: n = 0-750.

In one embodiment, a suitable linker is selected from Table 3a:

TABLE 3a Suitable Linkers

Note: n = 0-750

Commercial linkers are available from various suppliers such as Pierce or Quanta Biodesign including combinations of said linkers. The linkers may also be combined to produce more complex branched architectures accommodating from 1 to 6 targeting ligands and/or 1 to 6 peptides. In one embodiment, a combined targeting ligands and linkers has the structure T-L-1 as shown below:

Targeting Ligands

The compositions and peptide conjugates of the present invention may comprise a targeting ligand. The term “targeting ligand” as used herein refers to its meaning as is generally accepted in the art. The term generally refers to a moiety that confers some degree of target specificity to one or more cells, tissues, or organs, such as in a subject or organism and thus the ability to target such cells, tissues, or organs with a compound or composition of interest.

In some embodiments, this targeting ligand may direct the modular composition to a particular cell. For example, the targeting ligand may specifically or non-specifically bind with a molecule on the surface of a target cell. The targeting moiety can be a molecule with a specific affinity for a target cell. Targeting moieties can include antibodies directed against a protein found on the surface of a target cell, or the ligand or a receptor-binding portion of a ligand for a molecule found on the surface of a target cell. Examples and a further description of targeting ligands can be found in WO2009/126933, which is hereby incorporated by reference.

The targeting ligands are selected from the group consisting of an antibody, a ligand-binding portion of a receptor, a ligand for a receptor, an aptamer, D-galactose, N-acetyl-D-galactose (GalNAc), multivalent N-acytyl-D-galactose, D-mannose, cholesterol, a fatty acid, a lipoprotein, folate, thyrotropin, melanotropin, surfactant protein A, mucin, carbohydrate, multivalent lactose, multivalent galactose, N-acetyl-galactosamine, N-acetyl-glucosamine, multivalent mannose, multivalent fructose, glycosylated polyaminoacids, transferrin, bisphosphonate, polyglutamate, polyaspartate, a lipophilic moiety that enhances plasma protein binding, a steroid, bile acid, vitamin B12, biotin, an RGD peptide, an RGD peptide mimic, ibuprofen, naproxen, aspirin, folate, and analogs and derivatives thereof.

In one embodiment, a targeting ligand is selected from the group consisting of D-galactose, N-acetyl-D-galactose (GalNAc), GalNAc2, and GalNAc3, cholesterol, folate, and analogs and derivatives thereof.

In one embodiment, each occurance of the targeting ligand G of the above compositions and peptide conjugates is independently selected from Table 4.

TABLE 4 Suitable Ligands

wherein each X is independently —O—, —S—, —CH₂— or —NH—; and each n is independently 1, 2, 3, or 4,

In one embodiment, each occurance of G is independently selected from Table 4a.

TABLE 4a Suitable Ligands

wherein each X is independently —O—, —S—, —CH₂— or —NH—; and each n is independently 1, 2, 3, or 4.

In one embodiment, G of the above compositions and peptide conjugates comprises a ligand of the following formula:

wherein each n is independently an integer from 1 to 20.

In another embodiment, G of the above compositions and peptide conjugates comprises a ligand of the following formula:

wherein each n is independently an integer from 1 to 20.

Lipids

In one embodiment, R-(L)_(a)-(G)_(b) further comprises a lipid, either directly or through a suitable linker L.

In another embodiment, the peptide containing conjugate (P)_(c)-(L)_(d)-(G)_(e) further comprises a lipid either directly or through a suitable linker.

Lipids, such as cholesterol or fatty acids, when attached to highly hydrophilic molecules such as nucleic acids can substantially enhance plasma protein binding and consequently circulation half life. In addition, lipophilic groups can increase cellular uptake. For example, lipids can bind to certain plasma proteins, such as lipoproteins, which have consequently been shown to increase uptake in specific tissues expressing the corresponding lipoprotein receptors (e.g., LDL-receptor or the scavenger receptor SR-B1). Lipophilic conjugates can also be considered as a targeted delivery approach and their intracellular trafficking could potentially be further improved by the combination with endosomolytic agents.

Exemplary lipids that enhance plasma protein binding include, but are not limited to, sterols, cholesterol, fatty acids, cholic acid, lithocholic acid, dialkylglycerides, diacylglyceride, phospholipids, sphingolipids, adamantane acetic acid, 1-pyrene butyric acid, dihydrotestosterone, 1,3-bis-O(hexadecyl)glycerol, geranyloxyhexyl group, hexadecylglycerol, borneol, menthol, 1,3-propanediol, heptadecyl group, palmitic acid, myristic acid, O3-(oleoyl)lithocholic acid, O3-(oleoyl)cholenic acid, dimethoxytrityl, phenoxazine, aspirin, naproxen, ibuprofen, vitamin E and biotin etc. Examples of lipids can be found in WO2009/126933, which is hereby incorporated by reference.

In one embodiment, the lipid is cholesterol.

Solubilizing Agents

The R-(L)_(a)-(G)_(b) composition and/or the peptide containing conjugate (P)_(c)-(L)_(d)-(G)_(e) may further comprise one or more solubilizing agents that may enhance aqueous solubility, circulation half life and/or cellular uptake. These can include naturally occurring substances, such as a protein (e.g., human serum albumin (HSA), low-density lipoprotein (LDL), high-density lipoprotein (HDL), or globulin); or a carbohydrate (e.g., a dextran, pullulan, chitin, chitosan, inulin, cyclodextrin or hyaluronic acid). These moieties may also be a recombinant or synthetic molecule, such as a synthetic polymer or synthetic polyamino acids. Examples include polylysine (PLL), poly L-aspartic acid, poly L-glutamic acid, styrene-maleic acid anhydride copolymer, poly(L-lactide-co-glycolied) copolymer, divinyl ether-maleic anhydride copolymer, N-(2-hydroxypropyl)methacrylamide copolymer (HMPA), polyethylene glycol (PEG, e.g., PEG-0.5K, PEG-2K, PEG-5K, PEG-10K, PEG-12K, PEG-15K, PEG-20K, PEG-40K), methyl-PEG (mPEG), [mPEG]2, polyvinyl alcohol (PVA), polyurethane, poly(2 ethylacryllic acid), N-isopropylacrylamide polymers, or polyphosphazine. Examples and a further discription of solubilizing agents can be found in WO2009/126933, which is hereby incorporated by reference.

In one embodiment, the solubilizing group is PEG 0.5K to 30K.

In one embodiment, R-(L)_(a)-(G)_(b) comprises 1-4 targeting ligands. In another embodiment, R-(L)_(a)-(G)_(b) comprises 1-2 targeting ligands. In yet another embodiment, the composition comprises 1 targeting ligand.

In one embodiment, (P)_(c)-(L)_(d)-(G)_(e) comprises 1-6 peptides. In another embodiment, (P)_(c)-(L)_(d)-(G)_(e) comprises 1-4 peptides. In another embodiment, (P)_(c)-(L)_(d)-(G)_(e) comprises 1-2 peptides. In yet another embodiment, (P)_(c)-(L)_(d)-(G)_(e) comprises 1 peptide.

In one embodiment, the oligonucleotide is mRNA, and the ligand is attached to one or more terminal positions or through 2′-position of a nucleotide ribose ring.

In one embodiment, the oligonucleotide or siRNA is double stranded and there is one targeting ligand which is attached to the guide strand at a 2′-position of a nucleotide ribose ring, optionally through a suitable linker.

In one embodiment, the oligonucleotide or siRNA is double stranded and there is one targeting ligand which is attached to the guide strand at a terminal 3′ or 5′-position, optionally through a suitable linker.

In one embodiment, the oligonucleotide or siRNA is double stranded and there is one targeting ligand which is attached to the passenger strand at a 2′-position of a nucleotide ribose ring, optionally through a suitable linker.

In one embodiment, the oligonucleotide or siRNA is double stranded and there is one targeting ligand which is attached to the passenger strand at a terminal 3′ or 5′-position, optionally through a suitable linker.

In one embodiment, the oligonucleotide or siRNA is double stranded and two or more targeting ligands are attached to the guide strand at different 2′-positions of the ribose rings, optionally through a suitable linkers.

In one embodiment, the oligonucleotide or siRNA is double stranded and two or more targeting ligands are attached to two or more nucleotides of the guide strand, optionally through a suitable linkers, wherein the points of attachment are at different terminal 3′ and/or 5′-positions.

In one embodiment, the oligonucleotide or siRNA is double stranded and two or more targeting ligands are attached to two or more nucleotides of the passenger strand, optionally through a suitable linkers, wherein the points of attachment are at different terminal 3′ and/or 5′-positions.

In one embodiment, the oligonucleotide or siRNA is double stranded and two or more targeting ligands are attached to two or more nucleotides of both the guide strand and the passenger strand, optionally through a suitable linkers, wherein the points of attachment are at different terminal 3′ and/or 5′-positions.

In one embodiment, the oligonucleotide or siRNA is double stranded and optional targeting ligands, solubilizing agents, pharmacokinetics enhancing agents, lipids, and/or masking agents are attached to the same or different strands via linkers. In one embodiment, each linker is independently selected Table 3. In another embodiment, each linker is independently selected Table 3a.

To illustrate the invention, the invention features a modular composition, comprising an oligonucleotide or siRNA (R), one or more targeting ligands (G), one or more peptides (P), one or more optional linkers (L), and one or more optional ligands (X), solubilizing groups (X), pharmacokinetics enhancing agents (X), lipids (X), and/or masking agents (X). In one embodiment, the oligonucleotide is an siRNA. In another embodiment, the oligonucleotide is mRNA.

In one embodiment, the oligonucleotide composition has the formula:

G-R.

In one embodiment, the oligonucleotide composition has the formula:

G-L-R.

In one embodiment, the oligonucleotide composition has the formula:

G-L-R-X.

In one embodiment, the oligonucleotide composition has the formula:

G-L-R-L-X.

In one embodiment, the oligonucleotide composition has the formula:

G-R-L-P.

In one embodiment, the oligonucleotide composition has the formula:

G-L-R-L-P.

In one embodiment, the oligonucleotide composition has the formula:

In one embodiment, the oligonucleotide composition has the formula:

In one embodiment, a double stranded siRNA composition has the formula:

G-L-ds siRNA,

wherein the ds siRNA is a double stranded siRNA that comprises a passenger (sense) strand and a guide (antisense) strand, wherein the passenger strand nucleotide sequence is complimentary to the guide strand nucleotide sequence, and wherein the G-L- is attached to the 5′ end of the passenger strand. In one embodiment of the composition, the G-L- is attached to the 3′ end of the passenger strand. In one embodiment of the composition, the G-L- is attached to the 5′ end of the guide strand. In one embodiment of the composition, the G-L- is attached to the 3′ end of the guide strand.

When the oligonucleotide or siRNA is a double stranded oligonucleotide or siRNA, the “G-L-”, “P-L-” and “X-L-” may be located on the same strand or on different strands.

In one embodiment, a double stranded siRNA composition has the formula:

G-L-ds siRNA-L-P,

wherein the ds siRNA is a double stranded siRNA that comprises a passenger (sense) strand and a guide (antisense) strand, wherein the passenger strand nucleotide sequence is complimentary to the guide strand nucleotide sequence, wherein the G-L- is attached to the 5′ end of the passenger strand, and wherein the P-L- is attached to the 3′ end of the passenger strand. In one embodiment of the composition, the G-L- is attached to the 5′ end of the passenger strand, and the P-L- is attached to the 5′ end of the guide strand. In one embodiment of the composition, the G-L- is attached to the 3′ end of the guide strand, and the P-L- is attached to the 5′ end of the guide strand. In one embodiment of the composition, the G-L- is attached to the 3′ end of the guide strand, and the P-L- is attached to the 3′ end of the passenger strand.

In one embodiment, a double stranded siRNA composition has the formula:

wherein the ds siRNA is a double stranded siRNA that comprises a passenger (sense) strand and a guide (antisense) strand, wherein the passenger strand nucleotide sequence is complimentary to the guide strand nucleotide sequence, wherein the G-L- is attached to the 5′ end of the passenger strand, the P-L- is attached to the 3′ end of the passenger strand, and the X-L- is attached to the 3′ end of the guide strand. In one embodiment of the composition, the G-L- is attached to the 3′ end of the guide strand, the P-L- is attached to the 3′ end of the passenger strand, and the X-L- is attached to the 5′ end of the passenger strand. In one embodiment of the composition, the G-L- is attached to the 3′ end of the guide strand, the P-L- is attached to the 5′ end of the guide strand, and the X-L- is attached to the 5′ end of the passenger strand.

These examples are used as guidance. One skilled in the art will recognize that a variety of permutations for placing the desired components on the passenger and guide strand exist.

In some embodiments, when the oligonucleotide or siRNA is double-stranded and multiple “G-L”, “P-L” and/or “X-L” components are present, such multiple “G-L”, “P-L” and/or “X-L” components may all be present in one strand or both strands of the double stranded oligonucleotide or siRNA.

When multiple “G-L”, “P-L” and/or “X-L” components are present, they may all be the same or different.

In some embodiments, the “G-L”, “P-L” and “X-L” are on the same strand.

In some embodiments, the “G-L”, “P-L” and “X-L” are on the passenger strand.

In some embodiments, the “G-L”, “P-L” and “X-L” are on the guide strand.

In some embodiments, the “G-L”, “P-L” and “X-L” are on different strands.

In some embodiments, the “G-L” is on the passenger strand and the “P-L” is on the guide strand.

In some embodiments, the “G-L” is on the guide strand and the “P-L” is on the passenger strand.

In some embodiments, the “G-L”, “P-L” and “X-L” are on different strands but on the same terminal end of the double-stranded oligonucleotide or siRNA.

In some embodiments, the “G-L”, “P-L” and “X-L” are on different strands and on the opposite terminal ends of the double-stranded oligonucleotide or siRNA.

In some embodiments, one or more “G-L”, one or more “P-L” and/or one or more “X-L” of identical or different nature can be located on the guide strand or passenger starnd in the above embodiments.

In some embodiments, the “G-L” and “P-L” may be located on multiple terminal ends of either the passenger or guide strand and the “X-L” may be located on the remaining terminal ends of the passenger and guide strands.

The method can be performed in vitro, ex vivo or in vivo, e.g., to treat a subject identified as being in need of an oligonucleotide or siRNA. A subject in need of said oligonucleotide is a subject, e.g., a human, in need of having the expression of a gene or genes, e.g., a gene related to a disorder, downregulated or silenced.

In one aspect, the invention provides a method for inhibiting the expression of one or more genes. The method comprising contacting one or more cells with an effective amount of an oligonucleotide of the invention, wherein the effective amount is an amount that suppresses the expression of the one or more genes. The method can be performed in vitro, ex vivo or in vivo.

The methods and compositions of the invention can be used with any oligonucleotides or siRNAs known in the art. In addition, the methods and compositions of the invention can be used for the treatment of any disease or disorder known in the art, and for the treatment of any subject, e.g., any animal, any mammal, such as any human. One of ordinary skill in the art will also recognize that the methods and compositions of the invention may be used for the treatment of any disease that would benefit from downregulating or silencing a gene or genes.

One of ordinary skill in the art will further recognize that the methods and compositions of the invention may be used for expressing genes encoding proteins or polypeptides.

The methods and compositions of the invention may be used with any dosage and/or formulation described herein, or any dosage or formulation known in the art. In addition to the routes of administration described herein, a person skilled in the art will also appreciate that other routes of administration may be used to administer the modular composition of the invention.

Method of Treatment

In one aspect, the invention features a method of treating a subject at risk for or afflicted with a disease that may benefit from the administration of the modular composition of the invention. The method comprises administering the modular composition of the invention to a subject in need thereof, thereby treating the subject. The oligonucleotide that is administered will depend on the disease being treated. See WO2009/126933 for additional details regarding methods of treatments for specific indications.

Formulation

There are numerous methods for preparing conjugates of oligonucleotide and peptide compounds. The techniques should be familiar to those skilled in the art. A useful reference for such reactions is Bioconjugate Techniques, Hermanson, G. T., Academic Press, San Diego, Calif., 1996. Other references include WO2005/041859; WO2008/036825 and WO2009/126933.

Unless otherwise noted, the following terminology and definitions apply as used in the present application.

As used in this specification and the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the content clearly dictates otherwise. Thus, for example, reference to “a cell” includes a combination of two or more cells, and the like.

Any concentration range, percentage range, ratio range or integer range is to be understood to include the value of any integer within the recited range, and when appropriate, fractions thereof (such as one tenth and one hundredth of an integer), unless otherwise indicated.

“About” or “approximately,” as used herein, in reference to a number are generally taken to include numbers that fall within a range of 5% in either direction (greater than or less than) of the number unless otherwise stated or otherwise evident from the context (except where such number would exceed 100% of a possible value). Where ranges are stated, the endpoints are included within the range unless otherwise stated or otherwise evident from the context.

The phrase “biological system” as used herein refers to its meaning as is generally accepted in the art. The term generally refers to material, in a purified or unpurified form, from biological sources including, but not limited to, human or animal, wherein the system comprises the components required for RNAi activity. Thus, the phrase includes, for example, a cell, tissue, subject, or organism, or extract thereof. The term also includes reconstituted material from a biological source.

The term “cell” as used herein refers to its meaning as is generally accepted in the art. With reference to exemplary nucleic acid molecules of the invention, the term is used in its usual biological sense, and does not refer to an entire multicellular organism, e.g., specifically does not refer to a human being. The cell can be present in an organism, e.g., birds, plants and mammals, such as humans, cows, sheep, apes, monkeys, swine, dogs, and cats. The cell can be prokaryotic (e.g., bacterial cell) or eukaryotic (e.g., mammalian or plant cell). The cell can be of somatic or germ line origin, totipotent or pluripotent, dividing or non-dividing. The cell can also be derived from or can comprise a gamete or embryo, a stem cell, or a fully differentiated cell.

The terms “composition” or “formulation” as used herein refer to their generally accepted meaning in the art. These terms generally refer to a composition or formulation, such as in a pharmaceutically acceptable carrier or diluent, in a form suitable for administration, e.g., systemic or local administration, into a cell or subject, including, for example, a human. Suitable forms, in part, depend upon the use or the route of entry, for example oral, transdermal, inhalation, or by injection. Such forms should not prevent the composition or formulation from reaching a target cell. For example, compositions injected into the blood stream should be soluble. Other factors are known in the art, and include considerations such as toxicity and forms that prevent the composition or formulation from exerting its effect. As used herein, pharmaceutical formulations include formulations for human and veterinary use.

The term “including” (and any form thereof, such as “includes” and “include”), “comprising” (and any form thereof, such as “has” or “have”) or “containing” (and any form thereof such as “contains” or “contain”) are inclusive and open-ended and do not exclude additional, unrecited elements or method steps.

The terms “mammalian” or “mammal” as used herein refers to its meaning as is generally accepted in the art. The term generally refers to any warm blooded vertebrate species, such as a human, mouse, rat, dog, cat, hamster, guinea pig, rabbit, livestock, and the like.

The term “subject” as used herein refers to its meaning as is generally accepted in the art. The term generally refers an organism to which the nucleic acid molecules of the invention can be administered. A subject can be a mammal or mammalian cells, including a human or human cells. The term also refers to an organism, which is a donor or recipient of explanted cells or the cells themselves.

The phrase “systemic administration” as used herein refers to its meaning as is generally accepted in the art. The phrase generally refers in vivo systemic absorption or accumulation of drugs in the blood stream followed by distribution throughout the entire body.

The phrase “therapeutically effective amount” as used herein refers to its meaning as is generally accepted in the art. The term generally refers to the amount of the compound or composition that will elicit the biological or medical response of a cell, tissue, system, animal or human that is be sought by the researcher, veterinarian, medical doctor or other clinician. For example, if a given clinical treatment is considered effective when there is at least a 25% reduction in a measurable parameter associated with a disease or disorder, a therapeutically effective amount of a drug for the treatment of that disease or disorder is that amount necessary to effect at least a 25% reduction in that parameter.

EXAMPLES

The invention is further illustrated by the following examples, which should not be construed as further limiting. The contents of all references, pending patent applications and published patents, cited throughout this application are hereby expressly incorporated by reference. The siRNAs described herein were designed to target CTNNB1 (Beta Catenin).

Preparations of Compounds A9 and A10

TetraGalNAc Compounds A9 and A10 were prepared using steps and conditions as described in Scheme 1.

Synthesis of (2S)-2, 6-bis[bis (prop-2-yn-1-yl)amino]hexanoic acid (Compound A1)

Into a 2000-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of (2S)-2,6-diaminohexanoic acid (50 g, 342.03 mmol, 1.00 equiv) in acetonitrile (1000 mL) and heated to 50° C. To this was added potassium hydroxide (22.6 g, 0.4025 mol, 1.00 equiv, 85%). The resulting solution was stirred for 30 min. Then 3-bromoprop-1-yne (29.5 mL, 1.00 equiv) was added. The resulting solution was stirred for 1 hour at 50° C. Additional potassium hydroxide (22.6 g, 0.4025 mol, 1.00 equiv) was added to the solution and stirred for 30 min at 50° C. To this was added 3-bromoprop-1-yne (29.5 mL, 1.00 equiv). The resulting solution was stirred for 1 hour. To this was added potassium hydroxide (22.6 g, 0.4025 mol, 1.00 equiv) again. The resulting solution was stirred for 30 min at 50° C., followed by addition of more 3-bromoprop-1-yne (29.5 mL, 1.00 equiv). The resulting solution was stirred for 1 hour. To this was added potassium hydroxide (22.6 g, 0.4025 mol, 1.00 equiv). The resulting solution was stirred for 30 min. To this was added 3-bromoprop-1-yne (29.5 mL, 1.00 equiv). The resulting solution was stirred for 3 hours. The reaction mixture was cooled to 25° C. with a water/ice bath. The solid was filtered out. The filtrate was adjusted to pH 4 with HCl (6M). The solid was filtered out. The filtrate was concentrated under vacuum. The residue was applied onto a silica gel column and eluted with dichloromethane/methanol (100:1-25:1). This resulted in Compound A1 as an oil.

MS (ES, m/z): 297.2, [M−H]⁻¹HNMR(CDCl₃, 500 MHz ppm): 3.62 (d, J=2.0 Hz, 4H), 3.52-3.49 (m, 1H), 3.50 (d, J=2.4 Hz, 4H), 2.62 (t, J=7.1 Hz, 2H), 2.30 (t, J=2.4 Hz, 2H), 2.27 (t, J=2.4 Hz, 2H), 1.88-1.79 (m, 2H), 1.60-1.53 (m, 2H), 1.52-1.43 (m, 2H).

Synthesis of 2-(2-hydroxyethoxy)ethyl 4-methylbenzenesulfonate (Compound A3)

Into a 2000-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of 2-(2-hydroxyethoxy)ethan-1-ol (A2, 42.4 g, 399.55 mmol, 1.00 equiv) in dichloromethane (1000 mL) and triethylamine (27.9 g, 275.72 mmol, 0.25 equiv). To the above was added p-toluenesulfonyl chloride (19.1 g, 100.18 mmol, 0.50 equiv). After stirring for 1 h at 25° C., the resulting mixture was washed with 1×500 mL of aq. potassium hydrosulfate (1M) and 1×500 mL of aq. sodium bicarbonate (5%) respectively. The organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column and eluted with dichloromethane/methanol (100:1). This resulted in Compound A3 as an oil.

Synthesis of 2-(2-azidoethoxy)ethan-1-ol (Compound A4)

Into a 500-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of 2-(2-[[(4- 2-(2-hydroxyethoxy)ethyl 4-methylbenzenesulfonate (A3, 50 g, 192.08 mmol, 1.00 equiv) in N,N-dimethylformamide (250 mL). This was followed by the addition of sodium azide (18.79 g, 289.03 mmol, 1.50 equiv) at 25° C. The resulting solution was stirred for 5 h at 100° C. in an oil bath. The reaction mixture was cooled and filtered. The filtrate was concentrated under vacuum. The residual solution was diluted with 1000 mL of dichloromethane and washed with 1×500 mL of water. The organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column and eluted with dichloromethane/methanol (80:1). This resulted in Compound A4 as an oil.

¹HNMR (CDCl₃, 400 MHz ppm): 3.42-3.45 (t, J=4.8 Hz, 2H), 3.63-3.65 (t, J=4.8 Hz, 2H), 3.71-3.74 (t, J=4.8 Hz, 2H), 3.71-3.79 (m, 2H).

Synthesis of (3R,4R,5R,6R)-3-acetamido-6-(acetoxymethyl)tetrahydro-2H-pyran-2,4,5-triyl triacetate (Compound A6)

Into a 2000-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of (3R,4R,5R,6R)-3-amino-6-(hydroxymethyl)tetrahydro-2H-pyran-2,4,5-triol hydrochloride (A5, 120 g, 556.50 mmol, 1.00 equiv) in pyridine (1200 mL). This was followed by the addition of acetic anhydride (341.6 g, 3.35 mol, 6.00 equiv) dropwise with stirring at 0° C. The resulting solution was stirred overnight at 25° C. The reaction was then quenched by the addition of 8000 mL of water/ice. The solid was collected by filtration. This resulted in Compound A6 as a solid.

Synthesis of (3aR,5R,6R,7R,7aR)-5-(acetoxymethyl)-2-methyl-5,6,7,7a-tetrahydro-3aH-pyrano[3,2-d]oxazole-6,7-diyl diacetate (Compound A7)

Into a 2000-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of (3R,4R,5R,6R)-3-acetamido-6-(acetoxymethyl)tetrahydro-2H-pyran-2,4,5-triyl triacetate (A6, 30 g, 77.05 mmol, 1.00 equiv) in dichloromethane (1500 mL), then added iron (III) chloride (30 g, 184.95 mmol, 2.40 equiv). The resulting mixture was stirred for 2 h at 25° C. The reaction was then quenched by the addition of 1000 mL of water/ice. The organic layer was washed with 1×1000 mL of sodium aq. bicarbonate and 1×1000 mL of water, dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in Compound A7 as an oil.

¹HNMR (CDCl₃, 300 MHz ppm): 2.03 (s, 9H), 2.12 (s, 3H), 3.97-4.27 (m, 4H), 4.90-4.93 (m, J=3.3 Hz, 1H), 5.45-5.47 (t, J=3.0 Hz, 1H), 5.98-6.00 (d, J=6.6 Hz, 1H).

Synthesis of (2R,3R,4R,5R,6R)-5-acetamido-2-(acetoxymethyl)-6-[2-(2-azidoethoxy)ethoxy]tetrahydro-2H-pyran-3,4-diyl diacetate (Compound A8)

Into a 500-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of (3aR,5R,6R,7R,7aR)-5-(acetoxymethyl)-2-methyl-5,6,7,7a-tetrahydro-3aH-pyrano[3,2-d]oxazole-6,7-diyl diacetate (A7, 40 g, 121.47 mmol, 1.00 equiv) in 1,2-dichloroethane (200 mL), 2-(2-azidoethoxy)ethan-1-ol (A4, 23.89 g, 182.18 mmol, 1.50 equiv). To the above several 4A zeolite was added. The resulting mixture was stirred for 1 h at 25° C. Then trimethylsilyl trifluoromethanesulfonate (10.8 mL, 0.50 equiv) was added. After stirred overnight at 25° C., the reaction mixture was diluted with 500 mL of dichloromethane and washed with 1×500 mL of water, 1×500 mL of aq. sodium bicarbonate and 1×500 mL of water. The organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column and eluted with dichloromethane/methanol (100:1). This resulted in Compound A8 as an oil. MS (m/z): 461.1, [M+H]⁺

¹HNMR(CDCl₃, 500 MHz ppm) 5.78 (d, J=8.90 Hz, 1H), 5.36 (d, J=2.9 Hz, 1H), 5.22 (dd, J=11.2, 3.6 Hz, 1H), 4.77 (d, J=8.3 Hz, 1H), 4.19-4.12 (m, 2H), 4.11-4.05 (m, 1H), 3.98-3.92 (m, 2H), 3.82-3.78 (m, 1H), 3.71-3.63 (m, 4H), 3.49-3.38 (m, 2H), 2.16 (s, 3H), 2.05 (s, 3H), 2.01 (s, 3H), 1.97 (s, 3H).

Synthesis of (S)-2,6-bis(bis((1-(2-(2-(42R,3R,4R,5R,6R)-3-acetamido-4,5-diacetoxy-6-(acetoxymethyl)tetrahydro-2H-pyran-2-yl)oxy)ethoxy)ethyl)-1H-1,2,3-triazol-4-yl)methyl)amino)hexanoic acid (Compound A9, tetraGalNAc Acetate)

Into a 250-mL round bottom flask purged and maintained with an inert atmosphere of nitrogen was charged (2S)-2,6-bis [bis (prop-2-yn-1-yl) amino]hexanoic acid (A1, 1.0 g, 1.0 equiv), (2R,3R,4R,5R,6R)-5-acetamido-2-(acetoxymethyl)-6-[2-(2-azidoethoxy)ethoxy]tetrahydro-2H-pyran-3,4-diyl diacetate (A8, 9.26 g, 6.0 equiv), anhydrous THF 50 mL, CuBr.SMe₂ (0.138 g, 0.20 equiv), and anhydrous DBU (1.5 ml, 3.0 equiv) in respective order. The resulting solution was stirred for 16 h at room temperature, quenched with acetic acid (0.75 mL, 4.0 equiv), treated with MP-TMT resin (Part No: 801472, from Biotage) (9 g), aged at room temperature for 16 h, filtered, and concentrated the filtrate to a solid. The solid was then dissolved in CH₂Cl₂ (140 mL), and washed with AcOH/NaCl solution (140 mL). The AcOH/NaCl solution was prepared with 1 mL AcOH and 100 mL 20% NaCl solution. The bottom organic layer was concentrated, and purified on a SiO₂ column (220 g), eluting with CH₂Cl₂/MeOH. This resulted in Compound A9 as a solid (tetraGalNAc Acetate). MS (m/z): 2139.5, [M+H]⁺

Synthesis of (S)-2,6-bis(bis((1-(2-(2-(((2R,3R,4R,5R,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)ethoxy)ethyl)-1H-1,2,3-triazol-4-yl)methyl)amino)hexanoic acid (Compound A10, TetraGalNAc)

Into a 250-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen was charged (S)-2,6-bis(bis((1-(2-(2-(((2R,3R,4R,5R,6R)-3-acetamido-4,5-diacetoxy-6-(acetoxymethyl)tetrahydro-2H-pyran-2-yl)oxy)ethoxy)ethyl)-1H-1,2,3-triazol-4-yl)methyl)amino)hexanoic acid (A9, 6.9 g, 1.0 equiv), Na₂CO₃ (6.83 g, 20 eq), water (56 mL), and MeOH (32 mL) in respective order. The reaction was aged at room temperature for 16 h, concentrated to residue, redissolved in water (50 mL), and purified on Combiflash C18 gold reverse column (415 g), eluting with water/MeCN. After concentration under vacuum, the product was dissolved in minimum amount of water, and lyophilized to obtain Compound A10 (tetraGalNAc) as a solid.

MS (m/z): 1657 [M+Na]⁺

¹HNMR (D₂O, 500 MHz, ppm): 8.05 (s, 2H), 7.91 (s, 2H), 4.62 (t, J=5.0 Hz, 4H), 4.57 (t, J=5.0 Hz, 4H), 4.45-4.41 (d, J=8.6 Hz, 4H), 3.99-3.82 (m, 28H), 3.80-3.61 (m, 28H), 3.14 (t, J=7.1 Hz, 1H), 2.52 (broad s, 2H), 1.99 (s, 6H), 1.98 (s, 6H), 1.73 (m, 2H), 1.60 (m, 2H), 1.29 (m, 2H).

Preparation of B2 to B4

Conjugates B2 to B4 were prepared using steps and conditions as described in Scheme 2.

Synthesis of B2

HATU (30 mg, 0.080 mmol, 3 eq.) was dissolved in DMSO (400 uL) and added to a vial containing A10 (130 mg, 0.080 mmol, 3 eq.). The solution color turned pale yellow as the tetra GalNAc (A10) dissolved. DIEA (28 uL, 0.16 mmol, 6 eq.) was then added to the solution. Starting material passenger strand B1 (200 mg, 0.027 mmol, 1 eq.) was dissolved in water (400 uL) and diluted with DMSO (800 uL). The HATU solution was added to the RNA solution and mixed thoroughly. The reaction mixture was left at room temperature for 20 minutes. The reaction mixture was diluted with water to bring the total DMSO content to 5% and centrifugal dialyzed two times against water over a 3K membrane. Expected mass: 9147.5, found mass: 9149.0

Synthesis of B4

Guide strand (B3, 58 mg) was dissolved in water (5 mL) and added to a vial containing B2 (79 mg). The solution was thoroughly mixed and left at room temperature for 2 hours. The solution was freeze dried to afford the duplex as a solid.

Synthesis of Compounds C1 and C2

Compounds C1 to C2 were prepared using steps and conditions as described in Scheme 3.

Synthesis of N,N′-((2S,2′S,3S,3′S,4S,4′S,5S,5′S,6S,6′S)-2,2′-(((((4,4′-((((R)-6-(((1-(2-(2-(((2R,3R,4R,5R,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)ethoxy)ethyl)-1H-1,2,3-triazol-4-yl)methyl)((1-(2-(2-(((2 S,3 S,4 S,5 S,6 S)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)ethoxy)ethyl)-1H-1,2,3-triazol-4-yl)methyl)amino)-1-oxo-1-((2-(pyridin-2-yldisulfanyl)ethyl)amino)hexan-2-yl)azanediyl)bis(methylene))bis(1H-1,2,3-triazole-4,1-diyl))bis(ethane-2,1-diyl))bis(oxy))bis(ethane-2,1-diyl))bis(oxy))bis(4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3,2-diyl))diacetamide (Compound C1)

Into a 25-ml round bottom flask purged and maintained with an inert atmosphere of nitrogen was charged (S)-2,6-bis(bis((1-(2-(2-(((2R,3R,4R,5R,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)ethoxy)ethyl)-1H-1,2,3-triazol-4-yl)methyl)amino)hexanoic acid (A10, 500 mg, 1.0 equiv), dimethyl sulfoxide (1.5 ml), 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate (HATU, 465 mg, 2 equiv.), and N,N-diisopropylethylamine (267 ul, 2.5 equiv.) in respective order. The reaction was aged at room temperature for 5 minutes. To the reaction mixture was added 2-(pyridin-2-yldisulfanyl) ethanamine hydrochloride (272 mg, 2 equiv.) and N,N-diisopropylethylamine (267 ul, 2.5 equiv.) in dimethyl sulfoxide (1.5 ml). The resulting mixture was aged at room temperature for 15 minutes and then, purified using Reverse-Phase Chromatography on C18 column, eluting with 0.05% TFA (v/v) in water and 0.05% (v/v) TFA in acetonitrile. After lyophilization, the product, Compound C1 (TGN-spdp), was obtained as a solid. MS (m/z): 1804.3 [M+H]

Synthesis of TGN-S-S-peptide (Compound C2)

Into a 4-dram scintillation vial purged and maintained with an inert atmosphere of nitrogen was charged dry peptide (cglfgeieelieeglenlidwwng all (D) SEQ ID NO: 1527, 100 mg, 1 equiv.). To the reaction was added TGN-spdp (C1, 195 mg, 3 equiv.) in dimethylsulfoxide (3.2 ml). The resulting mixture was aged at room temperature for 1 hour and then, purified using Reverse-Phase Chromatography on C18 column, eluting with 0.05% TFA (v/v) in water and 0.05% (v/v) TFA in acetonitrile. After lyophilization, the product, Compound C2 (TGN-S-S-peptide), was obtained as a solid. MS: theoretical MW (4470.852)

m/z Charge Mass 923.8 3 2774.4 1116.12 4 4468.48 1488.47 3 4468.41

Synthesis of Compounds C3a, C3b, and C4

Compounds C3a, C3b and C4 were prepared using steps and conditions as described in Scheme 4.

Synthesis of Fmoc-ECL-peptide (C3a) and ECL-peptide (C3b)

Into a 4-dram scintillation vial purged and maintained with an inert atmosphere of nitrogen was charged peptide (glfgeieelieeglenlidwgng all (D), SEQ ID NO: 1074, 20 mg, 1 equiv.) in dimethyl sulfoxide (100 ul). To the reaction was added (9H-fluoren-9-yl)methyl ((S)-3-methyl-1-(((S)-1-((4-((((4-nitrophenoxy)carbonyl)oxy)methyl)phenyl)amino)-1-oxo-5-ureidopentan-2-yl)amino)-1-oxobutan-2-yl)carbamate (13.26 mg, 2.2 equiv.) in dimethylsulfoxide (100 ul). The resulting mixture was aged at room temperature for 1 hour and then, purified using Reverse-Phase Chromatography on C18 column, eluting with 0.05% TFA (v/v) in water and 0.05% (v/v) TFA in acetonitrile. After lyophilization, the product, Fmoc-ECL-peptide (C3a), was obtained as a solid. MS (m/z): 1587.7 (M+2, theoretical and observed)

Into a 4-dram scintillation vial was charged Fmoc-ECL-peptide (C3a, 16.29 mg, 1.0 equiv.) in dimethylformamide (500 ul) and piperidine (3.11 ul, 6 equiv.) in respective order. The resulting reaction was aged at room temperature for 1 hour and then, purified using Reverse-Phase Chromatography on C18 column, eluting with 0.05% TFA (v/v) in water and 0.05% (v/v) TFA in acetonitrile. After lyophilization, the product, ECL-peptide (C3b), was obtained as a solid. MS (m/z): 1476.6 (M+2, theoretical), 1476.90 (M+2, observed)

Synthesis of TGN-ECL-peptide (C4)

Into a 4-dram scintillation vial purged and maintained with an inert atmosphere of nitrogen was charged TetraGalNAc (A10, 25.2 mg, 4 equiv.) in dimethylformamide (193 ul), 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate (HATU, 2.2 mg, 1.5 equiv.), and N,N-Diisopropylethylamine (DIEA, 1.7 ul, 2.5 equiv.) in respective order. The reaction was aged at room temperature for 5 minutes. To the reaction mixture was added ECL-peptide (C3b, 11.37 mg, 1 equiv.) and N,N-diisopropylethylamine (1.7 ul, 2.5 equiv.) in dimethyl sulfoxide (193 ul). The resulting mixture was aged at room temperature for 15 minutes and then, purified using Reverse-Phase Chromatography on C18 column, eluting with 0.05% TFA (v/v) in water and 0.05% (v/v) TFA in Acetonitrile. After lyophilization, the product, TGN-ECL-peptide (C4), was obtained as a solid.

MS: theoretical MW (4568.86)

m/z charge mass 1140.33 4 4565.32 1520.78 3 4565.34

Synthesis of Compounds C5-C8

Compounds C5-C8 were prepared using steps and conditions as described in Scheme 5.

Synthesis of CDM-NHS (C5)

Into a 100-ml round bottom flask purged and maintained with an intert atmosphere of nitrogen was charged 3-(4-methyl-2,5-dioxo-2,5-dihydrofuran-3-yl)propanoic acid (2 g, 1 equiv.), 1-hydroxypyrrolidine-2,5-dione (NHS, 1.375 g, 1.1 equiv), 4-dimethylaminopyridine (DMAP, 0.066 g, 0.05 equiv.), and dichloromethane (50 ml) in respective order. To the reaction was added N,N′-dicyclohexylcarbodiimide (DCC, 11.95 ml, 1.0 M in DCM, 1.1 equiv.). The resulting reaction mixture was aged at room temperature overnight. The reaction mixture was filtered through a glass frit and concentrated in vacuo to give a tan solid which was dissolved in DCM and purified on a SiO₂ column (40 g), eluting with hexane/ethyl acetate to yield 2,5-dioxopyrrolidin-1-yl 3-(4-methyl-2,5-dioxo-2,5-dihydrofuran-3-yl)propanoate (CDM-NHS, C5) as a powder. MS (m/z): 282.1 [M+H]⁺

Synthesis of NH₂-TGN (C6)

Into a 4-dram scintillation vial purged and maintained with an inert atmosphere of nitrogen was charged TetraGalNAc (A10, 323 mg, 1 equiv.) in dimethyl sulfoxide (6.55 ml), 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium 3-oxid hexafluorophosphate (HATU, 229 mg, 3 equiv.), and N,N-diisopropylethylamine (DIEA, 420 ul, 12 equiv.) in respective order. The reaction was aged at room temperature for 5 minutes. To the reaction mixture was added (9H-fluoren-9-yl)methyl (2-aminoethyl)carbamate (Fmoc-ethyl-diamine, 283 mg, 5 equiv.) in dimethyl sulfoxide (266 ul). The resulting reaction mixture was aged at room temperature for 5 minutes and then, purified using Reverse-Phase Chromatography on C18 column, eluting with 0.05% TFA (v/v) in water and 0.05% (v/v) TFA in acetonitrile. After lyophilization, the resulting solid was dissolved in DMF (1 ml) and added piperidine (496 ul, 25 equiv.). The resulting reaction mixture was aged at room temperature for 30 minutes and then, purified using Reverse-Phase Chromatography on C18 column, eluting with 0.05% TFA (v/v) in water and 0.05% (v/v) TFA in acetonitrile. After lyophilization, the product (NH₂-TGN, C6) was obtained as a solid. MS (m/z): 1678.7 [M+H]⁺

Synthesis of CDM-TGN (C7)

Into a 10-ml round bottom flask purged and maintained with an inert atmosphere of nitrogen was charged NH₂-TGN (C6, 195 mg, 1 equiv.) in dimethyl sulfoxide (4 ml), CDM-NHS (C5, 131.2 mg, 4 equiv.) in dimethyl sulfoxide (1.64 ml), and N,N-diisopropylethylamine (DIEA, 60.9 ul, 3 equiv.) in respective order. The resulting reaction mixture was aged at room temperature for 1 hour and then, purified using Reverse-Phase Chromatography on C18 column, eluting with 0.05% TFA (v/v) in water and 0.05% (v/v) TFA in acetonitrile. After lyophilization, the product (CDM-TGN, C7) was obtained as a solid. MS (m/z): 1845.4 [M+H]⁺

Synthesis of TGN-CDM peptide (C8)

Into a 4-dram scintillation vial purged and maintained with an inert atmosphere of nitrogen was charged peptide (glfgeieelieeglenlidwgng all (D), SEQ ID NO: 1074, 2.8 mg, 1 equiv.), dimethyl sulfoxide (30 ul), 10% glucose (106 ul), 1M Hepes buffer (pH=10.66, 160 ul) and water (56 ul) in respective order, maintaining pH at 8.85. The resulting reaction mixture was added to CDM-TGN (C7, 16.22 mg, 8 equiv.). The final pH was brought up from 8.12 to 8.5 by adding 1M Hepes buffer (150 ul). The CDM masking on the peptide was confirmed by MS and CE. MS (m/z): 1091.02 [M+4], 4368.08 observed, 4,446.698 theoretical CE: retention time at 27.234 min

Synthesis of Compounds C9 and C10

Compounds C9-C10 were prepared using steps and conditions as described in Scheme 6.

Synthesis of 2K-PEG-spdp (C9)

Into a 4-dram scintillation vial purged and maintained with an inert atmosphere of nitrogen was charged NHS-dPEG₄₉-ester (200 mg, 1 equiv.) in dimethylsulfoxide (883 ul), 2-(pyridin-2-yldisulfanyl)ethanamine (SPDP, 40.2 mg, 2.5 equiv.) in dimethyl sulfoxide (31 ul), and N,N-diisopropylethylamine (DIEA, 136 ul, 9 equiv.) in respective order. The resulting reaction mixture was aged at room temperature for 30 minutes and then, purified using Reverse-Phase Chromatography on C18 column, eluting with 0.05% TFA (v/v) in water and 0.05% (v/v) TFA in Acetonitrile. After lyophilization, the product (2K-PEG-spdp, C9) was obtained as a solid. MS (m/z): 796.5 [M+3], 1185.8 [M+2]

Synthesis of 2K-PEG-S-S-peptide (C10)

Into a 4-dram scintillation vial purged and maintained with an inert atmosphere of nitrogen was charged peptide (cgffgeiaelieeglknlidwwng, all D, SEQ ID NO: 1692, 10 mg, 1 equiv.) and 2K-PEG-spdp (C9, 25.9 mg, 3 equiv.) in dimethyl sulfoxide (914 ul) in respective order. The resulting reaction was aged at room temperature for 1 hour and then, purified using Reverse-Phase Chromatography on C18 column, eluting with 0.05% TFA (v/v) in water and 0.05% (v/v) TFA in acetonitrile. After lyophilization, the product (2K-PEG-S-S-peptide, C10) was obtained as a solid. MS (m/z): 1675.1[M+3], 5028.3 observed, 5,014.81 theoretical

Formulation of Peptides and siRNA Conjugates

Materials—

Tris base used for buffer preparation was obtained from Promega Corporation (Madison, Wis.). Sucrose used for tonicity modification was acquired from Macron Fine Chemicals (Center Valley, Pa.). All water used for dilutions was distilled, deionized to a resistivity of 18.2 MΩ*cm and filtered through a 0.2 μm filter. Unless otherwise indicated, all other reagents were acquired and used as received from Sigma Aldrich (St. Louis, Mo.).

Formulation Preparation for Sequential Dosing Experiments In Vivo—

Prior to formulation, purified peptide and siRNA solutions were dehydrated by lyophilization at −42° C. under 40×10⁻³ mbar for 72 h. An isotonic sucrose formulation was prepared (292 mM, 10 wt %) and sterile filtered using aseptic handling techniques in a laminar flow hood. The lyophilized peptide product was either reconstituted in the sucrose formulation (for NHP model) or water (for mouse model) and allowed to equilibrate for 12 hr at 4° C. Rehydrated peptide was degassed via centrifugation (4000 g, 15 min) and sterile filtered using aseptic handling techniques. Following concentration analysis via UV and ICP spectroscopy (see Peptide Concentration Determination section), peptide stock solutions were diluted to target concentrations for dosing. Separately, siRNA was reconstituted in PBS and diluted to a target concentration for dosing. Both peptide and siRNA formulations were sterile filtered using aseptic handling techniques in a laminar flow hood. All formulations passed assessment for sterility and bioburden prior to dosing.

Formulation Preparation for Co-Dosing Experiments In Vivo—

Similar to previous formulations, purified peptide and siRNA solutions were dehydrated by lyophilization at −42° C. under 40×10⁻³ mbar for 72 h. Peptide and siRNA were separately rehydrated in isotonic sucrose or water for analysis in NHP or mouse models, respectively. Peptide and siRNA stocks were sterile filtered using aseptic handling techniques and stored in sterile vials. Following analytical characterization of peptide/siRNA concentration and purity, co-dosing formulation were prepared by aseptically mixing peptide, siRNA, and the isotonic sucrose solution to the target concentrations for dosing. For NHP studies, solution pH was adjusted through the addition of a sucrose-tris buffer to a final formulation composition of 292 mM sucrose, 50 mM Tris (pH 7.50). Peptide or siRNA-only experimental controls were prepared using identical procedures and formulation compositions as co-dosing groups. All formulations passed assessment for sterility and bioburden prior to dosing.

Analysis of Peptides and siRNA Conjugates

Peptide Concentration Determination

UV Absorbance—

The concentration of peptides containing Tryptophan (W), Tyrosine (Y) or Cystine residues was determined based on the summation of theoretical molar extinction coefficients of the UV active residues. UV absorbance was measured at 280 nm using a Spectramax M5e UV spectrophotometer (Molecular Devices, Sunnyvale, Calif.)

Inductively Coupled Plasma Spectroscopy—

The concentration of peptide in constructs containing disulfide linker chemistry was determined indirectly by quantitating the amount of sulfur present in the conjugate, using an iCAP 6000 Inductively Coupled Plasma (ICP) Spectrophotometer (Thermo Fischer, Pittsburgh, Pa.). Samples were diluted with water containing) ppm Germanium (Ge) (Ricca Chemical Company, Arlington Tx.) internal standard. After injection, the sample was introduced to Nebulizer source with RF Power 1350 W, Aux gas flow 0.5 L/min and Nebulizer Gas flow 0.65 L/min. Sulfur content was quantitated using an external standard calibration curve (ranging from 0 ppm to 2 ppm) prepared from NIST Sulfur (S) ICP standard containing 1 ppm Ge as an internal standard. Raw ppm value for sulfur was reported and final peptide concentration was calculated using the peptide to sulfur molar ratio.

siRNA Concentration Determination

Inductively Coupled Plasma Spectroscopy—

The concentration of siRNA in constructs was determined directly by quantitating the amount of phosphorus present in the nucleotide backbone, using an iCAP 6000 Inductively Coupled Plasma (ICP) Spectrophotometer (Thermo Fischer, Pittsburgh, Pa.). Samples were diluted with water containing 1 ppm Germanium (Ge) (Ricca Chemical Company, Arlington Tx.) internal standard. After injection, the sample was introduced to Nebulizer source with RF Power 1350 W, Aux gas flow 0.5 L/min and Nebulizer Gas flow 0.65 L/min. Phosphorus content was quantitated using an external standard calibration curve (ranging from 0 ppm to 3 ppm) prepared from NIST Phosphorus ICP standard containing 1 ppm Ge as an internal standard. Raw ppm value for phosphorus was reported and final siRNA concentration was calculated using the siRNA to phosphorus molar ratio.

siRNA Duplex Purity

siRNA duplex purity was determined by Capillary Electrophoresis using an Agilent G1600 (Agilent Technologies Sunnyvale, Ca.). Two techniques were employed based on siRNA conjugate composition: Capillary Zone Electrophoresis (CZE) or Micellar Electrokinetic Chromatography (MEKC). The sample was hydrodynamically injected onto a bare-fused silica capillary (Agilent extended light path 25 μm ID, 363 μm OD) at the anode end. The migration of analytes was initiated by applying positive 30 kV to the capillary. The siRNA signal was monitored by UV detection (abs. 260 nm). siRNA duplex purity was reported by area percent; excess single strand, functional duplex impurities and free peptide also reported. All siRNA duplex were >than 85% pure.

Peptide Purity Chromatographic Conditions

Peptide purity was determined by reverse-phase high performance liquid chromatography (RP-HPLC) using a Bio Basics 4 (150×4.6, 5μ particle size) column. The method conditions were as follows: Mobile Phase A: 0.1% trifluoroacetic acid (TFA) in water; Mobile Phase B: 0.1% TFA in acetonitrile; column temperature 60° C. and 1 ml/min flow rate. The gradient ramped from initial conditions of 5% B to 100% B in 60 minutes, followed by an 8 minute hold and returned to initial conditions. The peptide signal was monitored using fluorescence detection (ex. 280 nm and ex. 345 nm) and UV detection (abs. 214 nm). Peak purity was reported by area percent. All peptide conjugates were >70% pure.

Identity by Mass Spectrometry—Methodology and Data Analysis

Peptide and RNA samples were prepared for analysis by mass spectrometry by diluting stock sample solutions with DI water to create a working solution between 30-300 μg/mL. Mobile phase A (MPA) was an aqueous solution of 100 mM hexafluoroisopropanol (HFIP) and 8 mM Triethylamine (TEA), mobile phase B (MPB) was a 90:10 (v:v) acetonitrile:water mixture. Samples were analyzed by reverse-phase UPLC separation, followed by detection by Waters Synapt quadrupole time of flight (QToF) mass spectrometer operated in negative ion mode. The column used was a Waters Acquity UPLC BEH300 C₄ column (2.1 mm I.D.×100 mm length and the separation is performed at a flow rate of 0.35 mL/min at a column temperature of 65° C. The separation method starts with a 2 minute isocratic hold at 2% MPB, followed by a 5 minute gradient to 95% MPB, then another 2 minute isocratic hold at 95% MPB. The column is then equilibrated for 1 minute at 2% MPB prior to the next injection. The post-column eluent is introduced to the mass spectrometer by electrospray ionization. Data were collected ion negative ion mode between 650-4500 m/z, with no CID fragmentation. For all samples, a mass spectrum is obtained by averaging across the chromatographic peak in the MassLynx software. For RNA samples, raw mass spectra were deconvoluted from m/z to mass by using the MaxEnt1 algorithm in the MassLynx software. For peptide samples, the raw mass spectra were deconvoluted manually by determining charge states for all major peaks and calculating the resulting mass.

In Vitro DMD Assay

Cryopreserved primary Mouse hepatocytes (Bioreclamation, LLC) were placed into Collagen Type I coated 96-well plates at 25,000 cells per well in serum-containing InVitroGRO CP media (Bioreclamation, LLC) and allowed 5 hours to attach. Media was replaced with InVitroGRO HI media and cells were treated with siRNA-IV at 125 nM [siRNA] for 1 hour. Media was replaced with InVitroGRO HI media and cells were treated for approximately 16 hours with experimental Peptide conjugates at various concentrations to establish a dose-response curve. Peptide conjugates were washed out after 16 hours with InVitroGRO HI media and cells allowed to incubate for an additional 24 hours. Cells were then lysed and mRNA expression of the siRNA target was measured by RT-qPCR (Applied Biosystems Taqman reagents). mRNA silencing activity of each Peptide conjugate was expressed as an enhancement above the baseline activity of 125 nM siRNA-IV alone with respect to the untreated cells and all siRNA target Ct values were normalized to PPIB mRNA for each well (dddCt) and summarized.

The structure of TGN-S-S-peptide is shown below and the activity data is listed in Table 5 (siRNA-IV concentration was kept at 125 mM).

TABLE 5 In Vitro Data Targeted In vitro peptide dddCt Dose (vs. baseline Targeted peptide (nM) SCE dose) TGN-S-S-SEQ ID NO: 1747 (D) 5000 −1.98 TGN-S-S-SEQ ID NO: 1747 (D) 1000 −2.08 TGN-S-S-SEQ ID NO: 1747 (D) 200 −1.53 TGN-S-S-SEQ ID NO: 1747 (D) 40 −0.7 TGN-S-S-SEQ ID NO: 1747 (D) 8 −0.23 TGN-S-S-SEQ ID NO: 1748 (D) 5000 −2.01 TGN-S-S-SEQ ID NO: 1748 (D) 1000 −1.92 TGN-S-S-SEQ ID NO: 1748 (D) 200 −1.38 TGN-S-S-SEQ ID NO: 1748 (D) 40 −0.5 TGN-S-S-SEQ ID NO: 1748 (D) 8 −0.2 TGN-S-S-SEQ ID NO: 1749 (D) 5000 −0.11 TGN-S-S-SEQ ID NO: 1749 (D) 1000 −0.22 TGN-S-S-SEQ ID NO: 1749 (D) 200 −0.26 TGN-S-S-SEQ ID NO: 1749 (D) 40 −0.04 TGN-S-S-SEQ ID NO: 1749 (D) 8 0.02 TGN-S-S-SEQ ID NO: 1751 (D) 5000 0.01 TGN-S-S-SEQ ID NO: 1751 (D) 1000 −0.05 TGN-S-S-SEQ ID NO: 1751 (D) 200 0.09 TGN-S-S-SEQ ID NO: 1751 (D) 40 −0.12 TGN-S-S-SEQ ID NO: 1751 (D) 8 −0.1 TGN-S-S-SEQ ID NO: 1752 (D) 5000 −1.02 TGN-S-S-SEQ ID NO: 1752 (D) 1000 −0.95 TGN-S-S-SEQ ID NO: 1752 (D) 200 −0.89 TGN-S-S-SEQ ID NO: 1752 (D) 40 −0.48 TGN-S-S-SEQ ID NO: 1752 (D) 8 −0.25 TGN-S-S-SEQ ID NO: 1753 (D) 5000 −0.16 TGN-S-S-SEQ ID NO: 1753 (D) 1000 −0.18 TGN-S-S-SEQ ID NO: 1753 (D) 200 −0.2 TGN-S-S-SEQ ID NO: 1753 (D) 40 0.05 TGN-S-S-SEQ ID NO: 1753 (D) 8 0.15 TGN-S-S-SEQ ID NO: 1755 (D) 5000 −0.24 TGN-S-S-SEQ ID NO: 1755 (D) 1000 −0.49 TGN-S-S-SEQ ID NO: 1755 (D) 200 −0.38 TGN-S-S-SEQ ID NO: 1755 (D) 40 −0.24 TGN-S-S-SEQ ID NO: 1755 (D) 8 −0.01 TGN-S-S-SEQ ID NO: 1756 (D) 5000 −0.95 TGN-S-S-SEQ ID NO: 1756 (D) 1000 −1.05 TGN-S-S-SEQ ID NO: 1756 (D) 200 −0.76 TGN-S-S-SEQ ID NO: 1756 (D) 40 −0.4 TGN-S-S-SEQ ID NO: 1756 (D) 8 −0.15 TGN-S-S-SEQ ID NO: 1758 (D) 5000 −0.64 TGN-S-S-SEQ ID NO: 1758 (D) 1000 −0.77 TGN-S-S-SEQ ID NO: 1758 (D) 200 −0.38 TGN-S-S-SEQ ID NO: 1758 (D) 40 −0.02 TGN-S-S-SEQ ID NO: 1758 (D) 8 0.04 TGN-S-S-Seq-ID-88 (D) 5000 −1.7 TGN-S-S-SEQ ID NO: 1759 (D) 1000 −1.66 TGN-S-S-SEQ ID NO: 1759 (D) 200 −1.65 TGN-S-S-SEQ ID NO: 1759 (D) 40 −0.87 TGN-S-S-SEQ ID NO: 1759 (D) 8 −0.15 TGN-S-S-SEQ ID NO: 1760 (D) 5000 −1.46 TGN-S-S-SEQ ID NO: 1760 (D) 1000 −1.8 TGN-S-S-SEQ ID NO: 1760 (D) 200 −1.6 TGN-S-S-SEQ ID NO: 1760 (D) 40 −1.01 TGN-S-S-SEQ ID NO: 1760 (D) 8 −0.09 TGN-S-S-SEQ ID NO: 1761 (D) 5000 −0.11 TGN-S-S-SEQ ID NO: 1761 (D) 1000 −0.07 TGN-S-S-SEQ ID NO: 1761 (D) 200 −0.22 TGN-S-S-SEQ ID NO: 1761 (D) 40 −0.25 TGN-S-S-SEQ ID NO: 1761 (D) 8 0.08 TGN-S-S-SEQ ID NO: 1762 (D) 5000 −0.08 TGN-S-S-SEQ ID NO: 1762 (D) 1000 −0.39 TGN-S-S-SEQ ID NO: 1762 (D) 200 −0.17 TGN-S-S-SEQ ID NO: 1762 (D) 40 0.03 TGN-S-S-SEQ ID NO: 1762 (D) 8 −0.07 TGN-S-S-SEQ ID NO: 1763 (D) 5000 −1.29 TGN-S-S-SEQ ID NO: 1763 (D) 1000 −1.44 TGN-S-S-SEQ ID NO: 1763 (D) 200 −1.26 TGN-S-S-SEQ ID NO: 1763 (D) 40 −0.67 TGN-S-S-SEQ ID NO: 1763 (D) 8 −0.13 TGN-S-S-SEQ ID NO: 1764 (D) 5000 −0.75 TGN-S-S-SEQ ID NO: 1764 (D) 1000 −0.62 TGN-S-S-SEQ ID NO: 1764 (D) 200 −0.78 TGN-S-S-SEQ ID NO: 1764 (D) 40 −0.41 TGN-S-S-SEQ ID NO: 1764 (D) 8 −0.03 TGN-S-S-SEQ ID NO: 1765(D) 5000 −1.23 TGN-S-S-SEQ ID NO: 1765(D) 1000 −1.23 TGN-S-S-SEQ ID NO: 1765(D) 200 −0.88 TGN-S-S-SEQ ID NO: 1765(D) 40 −0.38 TGN-S-S-SEQ ID NO: 1765(D) 8 −0.04 TGN-S-S-SEQ ID NO: 1766 (D) 5000 −0.45 TGN-S-S-SEQ ID NO: 1766 (D) 1000 −0.49 TGN-S-S-SEQ ID NO: 1766 (D) 200 −0.31 TGN-S-S-SEQ ID NO: 1766 (D) 40 −0.16 TGN-S-S-SEQ ID NO: 1766 (D) 8 −0.05 TGN-S-S-SEQ ID NO: 1767(D) 5000 −0.36 TGN-S-S-SEQ ID NO: 1767(D) 1000 −0.4 TGN-S-S-SEQ ID NO: 1767(D) 200 −0.16 TGN-S-S-SEQ ID NO: 1767(D) 40 0 TGN-S-S-SEQ ID NO: 1767(D) 8 0.15 TGN-S-S-SEQ ID NO: 1768 (D) 5000 −1.73 TGN-S-S-SEQ ID NO: 1768 (D) 1000 −1.55 TGN-S-S-SEQ ID NO: 1768 (D) 200 −1.62 TGN-S-S-SEQ ID NO: 1768 (D) 40 −1.04 TGN-S-S-SEQ ID NO: 1768 (D) 8 −0.34 TGN-S-S-SEQ ID NO: 1769 (D) 5000 −1.83 TGN-S-S-SEQ ID NO: 1769 (D) 1000 −1.82 TGN-S-S-SEQ ID NO: 1769 (D) 200 −1.51 TGN-S-S-SEQ ID NO: 1769 (D) 40 −0.71 TGN-S-S-SEQ ID NO: 1769 (D) 8 −0.22 TGN-S-S-SEQ ID NO: 1770 (D) 5000 −1.4 TGN-S-S-SEQ ID NO: 1770 (D) 1000 −1.61 TGN-S-S-SEQ ID NO: 1770 (D) 200 −1.13 TGN-S-S-SEQ ID NO: 1770 (D) 40 −0.43 TGN-S-S-SEQ ID NO: 1770 (D) 8 −0.27 TGN-S-S-SEQ ID NO: 1771 (D) 5000 −1.97 TGN-S-S-SEQ ID NO: 1771 (D) 1000 −1.7 TGN-S-S-SEQ ID NO: 1771 (D) 200 −1.64 TGN-S-S-SEQ ID NO: 1771 (D) 40 −0.79 TGN-S-S-SEQ ID NO: 1771 (D) 8 −0.1 TGN-S-S-SEQ ID NO: 1772 (D) 5000 −0.08 TGN-S-S-SEQ ID NO: 1772 (D) 1000 −0.17 TGN-S-S-SEQ ID NO: 1772 (D) 200 −0.15 TGN-S-S-SEQ ID NO: 1772 (D) 40 −0.15 TGN-S-S-SEQ ID NO: 1772 (D) 8 0.03 TGN-S-S-SEQ ID NO: 1746 (D) 5000 −0.04 TGN-S-S-SEQ ID NO: 1746 (D) 1000 −0.09 TGN-S-S-SEQ ID NO: 1746 (D) 200 −0.07 TGN-S-S-SEQ ID NO: 1746 (D) 40 −0.09 TGN-S-S-SEQ ID NO: 1746 (D) 8 −0.01 TGN-S-S-SEQ ID NO: 1773(D) 5000 0.05 TGN-S-S-SEQ ID NO: 1773(D) 1000 0.04 TGN-S-S-SEQ ID NO: 1773(D) 200 −0.06 TGN-S-S-SEQ ID NO: 1773(D) 40 −0.03 TGN-S-S-SEQ ID NO: 1773(D) 8 0.03 TGN-S-S-SEQ ID NO: 1774 (D) 5000 0.37 TGN-S-S-SEQ ID NO: 1774 (D) 1000 0.17 TGN-S-S-SEQ ID NO: 1774 (D) 200 0.13 TGN-S-S-SEQ ID NO: 1774 (D) 40 0.14 TGN-S-S-SEQ ID NO: 1774 (D) 8 0.08 TGN-S-S-SEQ ID NO: 1775(D) 5000 −0.37 TGN-S-S-SEQ ID NO: 1775(D) 1000 −0.11 TGN-S-S-SEQ ID NO: 1775(D) 200 −0.14 TGN-S-S-SEQ ID NO: 1775(D) 40 −0.14 TGN-S-S-SEQ ID NO: 1775(D) 8 −0.1 TGN-S-S-SEQ ID NO: 1710 (D) 5000 −3.45 TGN-S-S-SEQ ID NO: 1710 (D) 1000 −3.1 TGN-S-S-SEQ ID NO: 1710 (D) 200 −2.2 TGN-S-S-SEQ ID NO: 1710 (D) 40 −0.71 TGN-S-S-SEQ ID NO: 1710 (D) 8 −0.14 TGN-S-S-SEQ ID NO: 1741 (L) 15000 −0.25 TGN-S-S-SEQ ID NO: 1741 (L) 3000 −0.4 TGN-S-S-SEQ ID NO: 1741 (L) 600 −0.08 TGN-S-S-SEQ ID NO: 1741 (L) 120 0.02 TGN-S-S-SEQ ID NO: 1741 (L) 24 0 TGN-S-S-SEQ ID NO: 1776 (D) 5000 −0.27 TGN-S-S-SEQ ID NO: 1776 (D) 1000 −0.29 TGN-S-S-SEQ ID NO: 1776 (D) 200 −0.17 TGN-S-S-SEQ ID NO: 1776 (D) 40 −0.12 TGN-S-S-SEQ ID NO: 1776 (D) 8 −0.09 TGN-S-S-SEQ ID NO: 1741 (D) 5000 −2.83 TGN-S-S-SEQ ID NO: 1741 (D) 1000 −2.34 TGN-S-S-SEQ ID NO: 1741 (D) 200 −1.36 TGN-S-S-SEQ ID NO: 1741 (D) 40 −0.67 TGN-S-S-SEQ ID NO: 1741 (D) 8 −0.23 TGN-S-S-SEQ ID NO: 1709 (D) 5000 −0.89 TGN-S-S-SEQ ID NO: 1709 (D) 1000 −1.03 TGN-S-S-SEQ ID NO: 1709 (D) 200 −0.92 TGN-S-S-SEQ ID NO: 1709 (D) 40 −0.62 TGN-S-S-SEQ ID NO: 1709 (D) 8 −0.43 TGN-S-S-SEQ ID NO: 1733 (D) 5000 −2.7 TGN-S-S-SEQ ID NO: 1733 (D) 1000 −2.64 TGN-S-S-SEQ ID NO: 1733 (D) 200 −1.39 TGN-S-S-SEQ ID NO: 1733 (D) 40 −0.87 TGN-S-S-SEQ ID NO: 1733 (D) 8 −0.51 TGN-S-S-SEQ ID NO: 1702 (D) 5000 −2.47 TGN-S-S-SEQ ID NO: 1702 (D) 1000 −2.1 TGN-S-S-SEQ ID NO: 1702 (D) 200 −1.75 TGN-S-S-SEQ ID NO: 1702 (D) 40 −1.09 TGN-S-S-SEQ ID NO: 1702 (D) 8 −0.68 TGN-S-S-SEQ ID NO: 1776 (D) 5000 −0.01 TGN-S-S-SEQ ID NO: 1776 (D) 1000 −0.21 TGN-S-S-SEQ ID NO: 1776 (D) 200 −0.26 TGN-S-S-SEQ ID NO: 1776 (D) 40 −0.1 TGN-S-S-SEQ ID NO: 1776 (D) 8 0.05 TGN-S-S-SEQ ID NO: 1741 (D) 5000 −0.27 TGN-S-S-SEQ ID NO: 1741 (D) 1000 −0.06 TGN-S-S-SEQ ID NO: 1741 (D) 200 0.08 TGN-S-S-SEQ ID NO: 1741 (D) 40 0.28 TGN-S-S-SEQ ID NO: 1741 (D) 8 −0.04 TGN-S-S-SEQ ID NO: 1738 (D) 5000 −2.19 TGN-S-S-SEQ ID NO: 1738 (D) 1000 −1.69 TGN-S-S-SEQ ID NO: 1738 (D) 200 −1.57 TGN-S-S-SEQ ID NO: 1738 (D) 40 −0.67 TGN-S-S-SEQ ID NO: 1738 (D) 8 −0.24 TGN-S-S-SEQ ID NO: 1740 (L) 5000 −0.06 TGN-S-S-SEQ ID NO: 1740 (L) 1000 −0.06 TGN-S-S-SEQ ID NO: 1740 (L) 200 −0.07 TGN-S-S-SEQ ID NO: 1740 (L) 40 0.13 TGN-S-S-SEQ ID NO: 1740 (L) 8 0 TGN-S-S-SEQ ID NO: 1741 (L) 5000 −0.58 TGN-S-S-SEQ ID NO: 1741 (L) 1000 0.98 TGN-S-S-SEQ ID NO: 1741 (L) 200 −0.25 TGN-S-S-SEQ ID NO: 1741 (L) 40 −0.11 TGN-S-S-SEQ ID NO: 1741 (L) 8 0.03 TGN-S-S-SEQ ID NO: 1740(D) 5000 −2.98 TGN-S-S-SEQ ID NO: 1740(D) 1000 −2.3 TGN-S-S-SEQ ID NO: 1740(D) 200 −1.29 TGN-S-S-SEQ ID NO: 1740(D) 40 −0.46 TGN-S-S-SEQ ID NO: 1740(D) 8 −0.19 TGN-S-S-SEQ ID NO: 1777 (D) 5000 0.09 TGN-S-S-SEQ ID NO: 1777 (D) 1000 −0.13 TGN-S-S-SEQ ID NO: 1777 (D) 200 −0.13 TGN-S-S-SEQ ID NO: 1777 (D) 40 0.28 TGN-S-S-SEQ ID NO: 1777 (D) 8 −0.18 TGN-S-S-Seq-ID-111 (D) 5000 −1.4 TGN-S-S-SEQ ID NO: 1778 (D) 1000 −1.54 TGN-S-S-SEQ ID NO: 1778 (D) 200 −0.91 TGN-S-S-SEQ ID NO: 1778 (D) 40 −0.57 TGN-S-S-SEQ ID NO: 1778 (D) 8 −0.38 TGN-S-S-SEQ ID NO: 1779(D) 5000 −1.51 TGN-S-S-SEQ ID NO: 1779(D) 1000 −1.52 TGN-S-S-SEQ ID NO: 1779(D) 200 −1.29 TGN-S-S-SEQ ID NO: 1779(D) 40 −0.24 TGN-S-S-SEQ ID NO: 1779(D) 8 −0.18 TGN-S-S-SEQ ID NO: 1780 (D) 5000 −3.2 TGN-S-S-SEQ ID NO: 1780 (D) 1000 0.18 TGN-S-S-SEQ ID NO: 1780 (D) 200 −2.83 TGN-S-S-SEQ ID NO: 1780 (D) 40 −1.05 TGN-S-S-SEQ ID NO: 1780 (D) 8 −0.11 TGN-S-S-SEQ ID NO: 1781 (D) 5000 0.01 TGN-S-S-SEQ ID NO: 1781 (D) 1000 −0.01 TGN-S-S-SEQ ID NO: 1781 (D) 200 0.03 TGN-S-S-SEQ ID NO: 1781 (D) 40 −0.02 TGN-S-S-SEQ ID NO: 1781 (D) 8 −0.01 TGN-S-S-SEQ-ID NO 115 (D) 5000 −0.17 TGN-S-S-SEQ ID NO: 1782 (D) 1000 −0.21 TGN-S-S-SEQ ID NO: 1782 (D) 200 −0.17 TGN-S-S-SEQ ID NO: 1782 (D) 40 0.43 TGN-S-S-SEQ ID NO: 1782 (D) 8 −0.14 TGN-S-S-SEQ ID NO: 1783 (D) 5000 −0.98 TGN-S-S-SEQ ID NO: 1783 (D) 1000 −1.03 TGN-S-S-SEQ ID NO: 1783 (D) 200 −0.61 TGN-S-S-SEQ ID NO: 1783 (D) 40 −0.31 TGN-S-S-SEQ ID NO: 1783 (D) 8 −0.15 TGN-S-S-SEQ ID NO: 1784 (D) 5000 −0.81 TGN-S-S-SEQ ID NO: 1784 (D) 1000 −1.01 TGN-S-S-SEQ ID NO: 1784 (D) 200 −0.57 TGN-S-S-SEQ ID NO: 1784 (D) 40 −0.22 TGN-S-S-SEQ ID NO: 1784 (D) 8 0.07 TGN-S-S-SEQ ID NO: 1785 (D) 5000 −2.03 TGN-S-S-SEQ ID NO: 1785 (D) 1000 0.84 TGN-S-S-SEQ ID NO: 1785 (D) 200 −1.68 TGN-S-S-SEQ ID NO: 1785 (D) 40 −0.44 TGN-S-S-SEQ ID NO: 1785 (D) 8 −0.1 TGN-S-S-SEQ ID NO: 1786 (D) 5000 0.18 TGN-S-S-SEQ ID NO: 1786 (D) 1000 0.06 TGN-S-S-SEQ ID NO: 1786 (D) 200 0.06 TGN-S-S-SEQ ID NO: 1786 (D) 40 0.13 TGN-S-S-SEQ ID NO: 1786 (D) 8 0.17 TGN-S-S-SEQ ID NO: 120 (D) 5000 −3.34 TGN-S-S-SEQ ID NO: 1788 (D) 1000 −2.8 TGN-S-S-SEQ ID NO: 1788 (D) 200 −1.91 TGN-S-S-SEQ ID NO: 1788 (D) 40 −0.18 TGN-S-S-SEQ ID NO: 1788 (D) 8 −0.17 TGN-S-S-SEQ ID NO: 1793 (D) 5000 −2.65 TGN-S-S-SEQ ID NO: 1793 (D) 1000 −2.75 TGN-S-S-SEQ ID NO: 1793 (D) 200 −2.36 TGN-S-S-SEQ ID NO: 1793 (D) 40 −1.04 TGN-S-S-SEQ ID NO: 1793 (D) 8 −0.02 TGN-S-S-SEQ ID NO: 1794 (D) 5000 −2.61 TGN-S-S-SEQ ID NO: 1794 (D) 1000 −2.71 TGN-S-S-SEQ ID NO: 1794 (D) 200 −2.22 TGN-S-S-SEQ ID NO: 1794 (D) 40 −0.8 TGN-S-S-SEQ ID NO: 1794 (D) 8 −0.09 TGN-S-S-SEQ ID NO: 1795 (D) 5000 −0.71 TGN-S-S-SEQ ID NO: 1795 (D) 1000 0.94 TGN-S-S-SEQ ID NO: 1795 (D) 200 −0.71 TGN-S-S-SEQ ID NO: 1795 (D) 40 −0.33 TGN-S-S-SEQ ID NO: 1795 (D) 8 −0.1 TGN-S-S-SEQ ID NO: 1796 (D) 5000 −1.81 TGN-S-S-SEQ ID NO: 1796 (D) 1000 −1.98 TGN-S-S-SEQ ID NO: 1796 (D) 200 −1.13 TGN-S-S-SEQ ID NO: 1796 (D) 40 −0.56 TGN-S-S-SEQ ID NO: 1796 (D) 8 0.05 TGN-S-S-SEQ ID NO: 1797 (D) 5000 0.24 TGN-S-S-SEQ ID NO: 1797 (D) 1000 0.05 TGN-S-S-SEQ ID NO: 1797 (D) 200 0.08 TGN-S-S-SEQ ID NO: 1797 (D) 40 0.41 TGN-S-S-SEQ ID NO: 1797 (D) 8 0 TGN-S-S-SEQ ID NO: 1798 (D) 5000 −0.18 TGN-S-S-SEQ ID NO: 1798 (D) 1000 −0.26 TGN-S-S-SEQ ID NO: 1798 (D) 200 −0.13 TGN-S-S-SEQ ID NO: 1798 (D) 40 −0.69 TGN-S-S-SEQ ID NO: 1798 (D) 8 −0.09 TGN-S-S-SSEQ ID NO: 1799(D) 5000 −2.22 TGN-S-S-SSEQ ID NO: 1799(D) 1000 −2.13 TGN-S-S-SSEQ ID NO: 1799(D) 200 −1.63 TGN-S-S-SSEQ ID NO: 1799(D) 40 −0.45 TGN-S-S-SSEQ ID NO: 1799(D) 8 0.03 TGN-S-S-SEQ ID NO: 1800 (D) 5000 −1.46 TGN-S-S-SEQ ID NO: 1800 (D) 1000 0.96 TGN-S-S-SEQ ID NO: 1800 (D) 200 −1.11 TGN-S-S-SEQ ID NO: 1800 (D) 40 −0.33 TGN-S-S-SEQ ID NO: 1800 (D) 8 0.14 TGN-S-S-SEQ ID NO: 1710 (D) 5000 −4.01 TGN-S-S-SEQ ID NO: 1710 (D) 1000 −3.47 TGN-S-S-SEQ ID NO: 1710 (D) 200 −2.74 TGN-S-S-SEQ ID NO: 1710 (D) 40 −1.06 TGN-S-S-SEQ ID NO: 1710 (D) 8 −0.13 TGN-S-S-SEQ ID NO: 1704 (D) 5000 −1.74 TGN-S-S-SEQ ID NO: 1704 (D) 1000 −1.76 TGN-S-S-SEQ ID NO: 1704 (D) 200 −1.28 TGN-S-S-SEQ ID NO: 1704 (D) 40 0.1 TGN-S-S-SEQ ID NO: 1704 (D) 8 −0.09 TGN-S-S-SEQ ID NO: 1733(D) 5000 −2.46 TGN-S-S-SEQ ID NO: 1733(D) 1000 −2.42 TGN-S-S-SEQ ID NO: 1733(D) 200 −1.42 TGN-S-S-SEQ ID NO: 1733(D) 40 −0.72 TGN-S-S-SEQ ID NO: 1733(D) 8 −0.19 TGN-S-S-SEQ ID NO: 1730 (D) 1000 −3.39 TGN-S-S-SEQ ID NO: 1730 (D) 200 −1 TGN-S-S-SEQ ID NO: 1730 (D) 40 −0.08 TGN-S-S-SEQ ID NO: 1730 (D) 8 0.11 TGN-S-S-SEQ ID NO: 1705 (D) 5000 −1.1 TGN-S-S-SEQ ID NO: 1705 (D) 1000 0.99 TGN-S-S-SEQ ID NO: 1705 (D) 200 −0.68 TGN-S-S-SEQ ID NO: 1705 (D) 40 −0.1 TGN-S-S-SEQ ID NO: 1705 (D) 8 0.16 TGN-S-S-SEQ ID NO: 1708 (L) 5000 0.14 TGN-S-S-SEQ ID NO: 1708 (L) 1000 0.07 TGN-S-S-SEQ ID NO: 1708 (L) 200 0.04 TGN-S-S-SEQ ID NO: 1708 (L) 40 0.06 TGN-S-S-SEQ ID NO: 1708 (L) 8 0 TGN-S-S-SEQ ID NO: 1711 (L) 5000 −0.18 TGN-S-S-SEQ ID NO: 1711 (L) 1000 −0.07 TGN-S-S-SEQ ID NO: 1711 (L) 200 −0.03 TGN-S-S-SEQ ID NO: 1711 (L) 40 −0.13 TGN-S-S-SEQ ID NO: 1711 (L) 8 −0.07 TGN-S-S-SEQ ID NO: 1712 (L) 5000 −0.2 TGN-S-S-SEQ ID NO: 1712 (L) 1000 0 TGN-S-S-SEQ ID NO: 1712 (L) 200 −0.08 TGN-S-S-SEQ ID NO: 1712 (L) 40 0.07 TGN-S-S-SEQ ID NO: 1712 (L) 8 0.03 TGN-S-S-SEQ ID NO: 1713 (L) 5000 0 TGN-S-S-SEQ ID NO: 1713 (L) 1000 −0.04 TGN-S-S-SEQ ID NO: 1713 (L) 200 0.15 TGN-S-S-SEQ ID NO: 1713 (L) 40 0.21 TGN-S-S-SEQ ID NO: 1713 (L) 8 0.21 TGN-S-S-SEQ ID NO: 1715 (L) 5000 −0.3 TGN-S-S-SEQ ID NO: 1715 (L) 1000 −0.1 TGN-S-S-SEQ ID NO: 1715 (L) 200 −0.04 TGN-S-S-SEQ ID NO: 1715 (L) 40 −0.02 TGN-S-S-SEQ ID NO: 1715 (L) 8 0.07 TGN-S-S-Seq-ID-37 (L) 5000 −0.79 TGN-S-S-Seq-ID-37 (L) 1000 −0.19 TGN-S-S-Seq-ID-37 (L) 200 −0.01 TGN-S-S-Seq-ID-37 (L) 40 0.14 TGN-S-S-Seq-ID-37 (L) 8 0.02 TGN-S-S-Seq-ID-40 (L) 5000 −0.2 TGN-S-S-Seq-ID-40 (L) 1000 −0.12 TGN-S-S-Seq-ID-40 (L) 200 −0.12 TGN-S-S-Seq-ID-40 (L) 40 −0.07 TGN-S-S-Seq-ID-40 (L) 8 −0.14 TGN-S-S-Seq-ID-41 (L) 5000 −0.11 TGN-S-S-Seq-ID-41 (L) 1000 −0.2 TGN-S-S-Seq-ID-41 (L) 200 −0.06 TGN-S-S-Seq-ID-41 (L) 40 −0.14 TGN-S-S-Seq-ID-41 (L) 8 −0.11 TGN-S-S-Seq-ID-45 (L) 5000 −0.26 TGN-S-S-Seq-ID-45 (L) 1000 −0.01 TGN-S-S-Seq-ID-45 (L) 200 −0.08 TGN-S-S-Seq-ID-45 (L) 40 0.04 TGN-S-S-Seq-ID-45 (L) 8 −0.14 TGN-S-S-Seq-ID-50 (D) 5000 −0.3 TGN-S-S-Seq-ID-50 (D) 1000 −0.17 TGN-S-S-Seq-ID-50 (D) 200 0.07 TGN-S-S-Seq-ID-50 (D) 40 0.03 TGN-S-S-Seq-ID-50 (D) 8 −0.01 TGN-S-S-Seq-ID-53 (L) 5000 0.01 TGN-S-S-Seq-ID-53 (L) 1000 −0.02 TGN-S-S-Seq-ID-53 (L) 200 −0.11 TGN-S-S-Seq-ID-53 (L) 40 −0.08 TGN-S-S-Seq-ID-53 (L) 8 −0.11 TGN-S-S-Seq-ID-54 (L) 5000 0.07 TGN-S-S-Seq-ID-54 (L) 1000 −0.03 TGN-S-S-Seq-ID-54 (L) 200 −0.16 TGN-S-S-Seq-ID-54 (L) 40 −0.07 TGN-S-S-Seq-ID-54 (L) 8 0.03 TGN-S-S-Seq-ID-55 (L) 5000 −0.01 TGN-S-S-Seq-ID-55 (L) 1000 0.05 TGN-S-S-Seq-ID-55 (L) 200 0.12 TGN-S-S-Seq-ID-55 (L) 40 0.08 TGN-S-S-Seq-ID-55 (L) 8 0.11 TGN-S-S-Seq-ID-56 (L) 5000 −0.58 TGN-S-S-Seq-ID-56 (L) 1000 −0.08 TGN-S-S-Seq-ID-56 (L) 200 −0.12 TGN-S-S-Seq-ID-56 (L) 40 0.05 TGN-S-S-Seq-ID-56 (L) 8 0.02 TGN-S-S-Seq-ID-57 (L) 5000 0.09 TGN-S-S-Seq-ID-57 (L) 1000 0.1 TGN-S-S-Seq-ID-57 (L) 200 0.02 TGN-S-S-Seq-ID-57 (L) 40 0 TGN-S-S-Seq-ID-57 (L) 8 0.1 TGN-S-S-Seq-ID-58 (D) 5000 −0.3 TGN-S-S-Seq-ID-58 (D) 1000 −0.26 TGN-S-S-Seq-ID-58 (D) 200 −0.25 TGN-S-S-Seq-ID-58 (D) 40 −0.03 TGN-S-S-Seq-ID-58 (D) 8 −0.05 TGN-S-S-Seq-ID-59 (D) 5000 0.25 TGN-S-S-Seq-ID-59 (D) 1000 0.17 TGN-S-S-Seq-ID-59 (D) 200 −0.02 TGN-S-S-Seq-ID-59 (D) 40 −0.03 TGN-S-S-Seq-ID-59 (D) 8 −0.13 TGN-S-S-Seq-ID-61 (D) 5000 −0.55 TGN-S-S-Seq-ID-61 (D) 1000 0 TGN-S-S-Seq-ID-61 (D) 200 0.01 TGN-S-S-Seq-ID-61 (D) 40 0.08 TGN-S-S-Seq-ID-61 (D) 8 0.13 TGN-S-S-Seq-ID-65 (D) 5000 −2.68 TGN-S-S-Seq-ID-65 (D) 1000 −1.88 TGN-S-S-Seq-ID-65 (D) 200 −1.48 TGN-S-S-Seq-ID-65 (D) 40 −0.73 TGN-S-S-Seq-ID-65 (D) 8 0 TGN-S-S-Seq-ID-29 (D) 5000 −0.72 TGN-S-S-Seq-ID-29 (D) 1000 −0.52 TGN-S-S-Seq-ID-29 (D) 200 −0.44 TGN-S-S-Seq-ID-29 (D) 40 −0.12 TGN-S-S-Seq-ID-29 (D) 8 0.05 TGN-S-S-Seq-ID-28 (D) 5000 −1.67 TGN-S-S-Seq-ID-28 (D) 1000 −1.65 TGN-S-S-Seq-ID-28 (D) 200 −1.47 TGN-S-S-Seq-ID-28 (D) 40 −1.14 TGN-S-S-Seq-ID-28 (D) 8 −0.27 TGN-S-S-Seq-ID-27 (D) 5000 −0.65 TGN-S-S-Seq-ID-27 (D) 1000 −0.61 TGN-S-S-Seq-ID-27 (D) 200 −0.53 TGN-S-S-Seq-ID-27 (D) 40 −0.38 TGN-S-S-Seq-ID-27 (D) 8 −0.05 TGN-S-S-Seq-ID-26 (D) 5000 −0.69 TGN-S-S-Seq-ID-26 (D) 1000 0.12 TGN-S-S-Seq-ID-26 (D) 200 0.21 TGN-S-S-Seq-ID-26 (D) 40 0.1 TGN-S-S-Seq-ID-26 (D) 8 0.1 TGN-S-S-Seq-ID-25 (D) 5000 −1.72 TGN-S-S-Seq-ID-25 (D) 1000 0.01 TGN-S-S-Seq-ID-25 (D) 200 −0.13 TGN-S-S-Seq-ID-25 (D) 40 0.2 TGN-S-S-Seq-ID-25 (D) 8 −0.06 TGN-S-S-SEQ ID NO: 1710 (D) 5000 −3.12 TGN-S-S-SEQ ID NO: 1710 (D) 1000 −2.83 TGN-S-S-SEQ ID NO: 1710 (D) 200 −2 TGN-S-S-SEQ ID NO: 1710 (D) 40 −1.04 TGN-S-S-SEQ ID NO: 1710 (D) 8 −0.2 TGN-S-S-SEQ ID NO: 1732(D) 3125 0.67 TGN-S-S-SEQ ID NO: 1732(D) 625 0.66 TGN-S-S-SEQ ID NO: 1732(D) 125 0.47 TGN-S-S-SEQ ID NO: 1732(D) 25 0.47 TGN-S-S-SEQ ID NO: 1078 (D) 3125 −1.06 TGN-S-S-SEQ ID NO: 1078 (D) 625 −0.96 TGN-S-S-SEQ ID NO: 1078 (D) 125 −0.82 TGN-S-S-SEQ ID NO: 1078 (D) 25 −0.34 TGN-S-S-SEQ ID NO: 1633 (D) 3125 −0.2 TGN-S-S-SEQ ID NO: 1633 (D) 625 −0.2 TGN-S-S-SEQ ID NO: 1633 (D) 25 −0.33 TGN-S-S-SEQ ID NO: 1703 (D) 3125 −0.57 TGN-S-S-SEQ ID NO: 1703 (D) 625 −0.43 TGN-S-S-SEQ ID NO: 1703 (D) 125 −0.38 TGN-S-S-SEQ ID NO: 1703 (D) 25 −0.09 TGN-S-S-SEQ ID NO: 1654 (D) 3125 −1.48 TGN-S-S-SEQ ID NO: 1654 (D) 625 −1.3 TGN-S-S-SEQ ID NO: 1654 (D)) 125 −1.05 TGN-S-S-SEQ ID NO: 1654 (D) 25 −0.39 TGN-S-S-SEQ ID NO: 1631 (D) 3125 −0.37 TGN-S-S-SEQ ID NO: 1631 (D) 625 0.07 TGN-S-S-SEQ ID NO: 1631 (D) 125 0.25 TGN-S-S-SEQ ID NO: 1704 (D) 3125 −0.39 TGN-S-S-SEQ ID NO: 1704 (D) 625 −0.56 TGN-S-S-SEQ ID NO: 1704 (D) 125 −0.32 TGN-S-S-SEQ ID NO: 1704 (D) 25 −0.08 TGN-S-S-SEQ ID NO: 1653 (D) 3125 −2.46 TGN-S-S-SEQ ID NO: 1653 (D) 625 −1.97 TGN-S-S-SEQ ID NO: 1653 (D) 125 −1.45 TGN-S-S-SEQ ID NO: 1653 (D) 25 −0.76 TGN-S-S-SEQ ID NO: 1717 (L) 3125 0.15 TGN-S-S-SEQ ID NO: 1717 (L) 625 0.37 TGN-S-S-SEQ ID NO: 1717 (L) 25 0.61 TGN-S-S-SEQ ID NO: 1705 (D) 3125 −0.17 TGN-S-S-SEQ ID NO: 1705 (D) 625 −0.69 TGN-S-S-SEQ ID NO: 1705 (D) 125 −0.21 TGN-S-S-SEQ ID NO: 1705 (D) 25 −0.06 TGN-S-S-SEQ ID NO: 1706 (D) 3125 −1.01 TGN-S-S-SEQ ID NO: 1706 (D) 625 −1.05 TGN-S-S-SEQ ID NO: 1706 (D) 125 −0.95 TGN-S-S-SEQ ID NO: 1706 (D) 25 −0.77 TGN-S-S-SEQ ID NO: 1730 (D) 3125 −3.38 TGN-S-S-SEQ ID NO: 1730 (D) 625 −0.67 TGN-S-S-SEQ ID NO: 1730 (D) 125 0.15 TGN-S-S-SEQ ID NO: 1730 (D) 25 0.44 TGN-S-S-SEQ ID NO: 1707 (D) 3125 −0.39 TGN-S-S-SEQ ID NO: 1707 (D) 625 −0.54 TGN-S-S-SEQ ID NO: 1707 (D) 125 −0.21 TGN-S-S-SEQ ID NO: 1707 (D) 25 −0.35 TGN-S-S-SEQ ID NO: 1647 (D) 3125 −0.21 TGN-S-S-SEQ ID NO: 1647 (D) 625 −0.41 TGN-S-S-SEQ ID NO: 1647 (D) 125 −0.32 TGN-S-S-SEQ ID NO: 1647 (D) 25 −0.05 TGN-S-S-SEQ ID NO: 1720 (L) 625 −0.57 TGN-S-S-SEQ ID NO: 1720 (L) 125 0.13 TGN-S-S-SEQ ID NO: 1720 (L) 25 0.04 TGN-S-S-SEQ ID NO: 1733 (D) 3125 −1.93 TGN-S-S-SEQ ID NO: 1733 (D) 625 −1.92 TGN-S-S-SEQ ID NO: 1733 (D) 125 −1.16 TGN-S-S-SEQ ID NO: 1733 (D) 25 −0.85 TGN-S-S-SEQ ID NO: 1701 (D) 3125 −1.69 TGN-S-S-SEQ ID NO: 1701 (D) 625 −1.46 TGN-S-S-SEQ ID NO: 1701 (D) 125 −1.55 TGN-S-S-SEQ ID NO: 1701 (D) 25 −0.58 TGN-S-S-SEQ ID NO: 1518 (L) 3125 0.19 TGN-S-S-SEQ ID NO: 1518 (L) 625 0.3 TGN-S-S-SEQ ID NO: 1518 (L) 125 0.37 TGN-S-S-SEQ ID NO: 1518 (L) 25 0.54 TGN-S-S-SEQ ID NO: 1734 (D) 3125 −1.14 TGN-S-S-SEQ ID NO: 1734 (D) 625 −0.86 TGN-S-S-SEQ ID NO: 1734 (D) 125 −0.42 TGN-S-S-SEQ ID NO: 1734 (D) 25 −0.2 TGN-S-S-SEQ ID NO: 1628 (D) 3125 −2.24 TGN-S-S-SEQ ID NO: 1628 (D) 625 −1.64 TGN-S-S-SEQ ID NO: 1628 (D) 125 −1.17 TGN-S-S-SEQ ID NO: 1628 (D) 25 −0.54 TGN-S-SEQ ID NO: 1517 (L) 3125 0.33 TGN-S-SEQ ID NO: 1517 (L) 625 0.48 TGN-S-SEQ ID NO: 1517 (L) 125 0.49 TGN-S-SEQ ID NO: 1517 (L) 25 0.54 TGN-S-S-SEQ ID NO: 1652 (D) 15625 −2.03 TGN-S-S-SEQ ID NO: 1652 (D) 3125 −1.6 TGN-S-S-SEQ ID NO: 1652 (D) 625 −1.5 TGN-S-S-SEQ ID NO: 1652 (D) 125 −1.27 TGN-S-S-SEQ ID NO: 1701 (D) 15625 −2.15 TGN-S-S-SEQ ID NO: 1701 (D) 3125 −1.65 TGN-S-S-SEQ ID NO: 1701 (D) 625 −1.35 TGN-S-S-SEQ ID NO: 1701 (D) 125 −1.14 TGN-S-S-SEQ ID NO: 1078(D) 15625 −1.44 TGN-S-S-SEQ ID NO: 1078(D) 3125 −1.17 TGN-S-S-SEQ ID NO: 1078(D) 625 −1.24 TGN-S-S-SEQ ID NO: 1078(D) 125 −1.04 TGN-S-S-SEQ ID NO: 1651 (D) 15625 −1.48 TGN-S-S-SEQ ID NO: 1651 (D) 3125 −1.55 TGN-S-S-SEQ ID NO: 1651 (D) 625 −1.11 TGN-S-S-SEQ ID NO: 1651 (D) 125 −0.84 TGN-S-S-SEQ ID NO: 1628 (D) 15625 −2.67 TGN-S-S-SEQ ID NO: 1628 (D) 3125 −2.15 TGN-S-S-SEQ ID NO: 1628 (D) 625 −1.86 TGN-S-S-SEQ ID NO: 1628 (D) 125 −1.17 TGN-S-S-SEQ ID NO: 1662 15625 −0.45 TGN-S-S-SEQ ID NO: 1662 3125 −0.48 TGN-S-S-SEQ ID NO: 1662 625 −0.47 TGN-S-S-SEQ ID NO: 1662 125 −0.31 TGN-S-S-SEQ ID NO: 1650 (D) 15625 −0.57 TGN-S-S-SEQ ID NO: 1650 (D) 3125 −0.21 TGN-S-S-SEQ ID NO: 1650 (D) 625 −0.45 TGN-S-S-SEQ ID NO: 1650 (D) 125 −0.33 TGN-S-S-SEQ ID NO: 1633(D) 15625 −0.69 TGN-S-S-SEQ ID NO: 1633(D) 3125 −0.37 TGN-S-S-SEQ ID NO: 1633(D) 625 −0.57 TGN-S-S-SEQ ID NO: 1633(D) 125 −0.39 TGN-S-S-SEQ ID NO: 1696 15625 −0.54 TGN-S-S-SEQ ID NO: 1696 3125 −0.4 TGN-S-S-SEQ ID NO: 1696 625 −0.59 TGN-S-S-SEQ ID NO: 1696 125 −0.41 TGN-S-S-SEQ ID NO: 1632 (D) 15625 −0.47 TGN-S-S-SEQ ID NO: 1632 (D) 3125 −0.19 TGN-S-S-SEQ ID NO: 1632 (D) 625 −0.44 TGN-S-S-SEQ ID NO: 1632 (D) 125 −0.29 TGN-S-S-SEQ ID NO: 1657 (D) 15625 −0.56 TGN-S-S-SEQ ID NO: 1657 (D) 3125 −0.4 TGN-S-S-SEQ ID NO: 1657 (D) 625 −0.49 TGN-S-S-SEQ ID NO: 1657 (D) 125 −0.42 TGN-S-S-SEQ ID NO: 1634 (D) 15625 −0.74 TGN-S-S-SEQ ID NO: 1634 (D) 3125 −0.3 TGN-S-S-SEQ ID NO: 1634 (D) 625 −0.41 TGN-S-S-SEQ ID NO: 1634 (D) 125 −0.3 TGN-S-S-SEQ ID NO: 1660(D) 15625 −0.7 TGN-S-S-SEQ ID NO: 1660(D) 3125 −0.69 TGN-S-S-SEQ ID NO: 1660(D) 625 −0.9 TGN-S-S-SEQ ID NO: 1660(D) 125 −0.57 TGN-S-S-SEQ ID NO: 1649 (D) 15625 −0.77 TGN-S-S-SEQ ID NO: 1649 (D) 3125 −0.61 TGN-S-S-SEQ ID NO: 1649 (D) 625 −0.48 TGN-S-S-SEQ ID NO: 1649 (D) 125 −0.3 TGN-S-S-SEQ ID NO: 1631 (D) 15625 −2.11 TGN-S-S-SEQ ID NO: 1631 (D) 3125 −0.45 TGN-S-S-SEQ ID NO: 1631 (D) 625 −0.3 TGN-S-S-SEQ ID NO: 1631 (D) 125 −0.19 TGN-S-S-SEQ ID NO: 1654 (D) 15625 −1.61 TGN-S-S-SEQ ID NO: 1654 (D) 3125 −1.48 TGN-S-S-SEQ ID NO: 1654 (D) 625 −1.08 TGN-S-S-SEQ ID NO: 1654 (D) 125 −1.05 TGN-S-S-SEQ ID NO: 1648 (D) 15625 −0.59 TGN-S-S-SEQ ID NO: 1648 (D) 3125 −0.39 TGN-S-S-SEQ ID NO: 1648 (D) 625 −0.57 TGN-S-S-SEQ ID NO: 1648 (D) 125 −0.27 TGN-S-S-SEQ ID NO: 255 (D) 625 −1.59 TGN-S-S-SEQ ID NO: 255 (D) 125 −0.37 TGN-S-S-SEQ ID NO: 1653 (D) 15625 −2.13 TGN-S-S-SEQ ID NO: 1653 (D) 3125 −1.92 TGN-S-S-SEQ ID NO: 1653 (D) 625 −1.53 TGN-S-S-SEQ ID NO: 1653 (D) 125 −1.31 TGN-S-S-SEQ ID NO: 1647 (D) 15625 −0.68 TGN-S-S-SEQ ID NO: 1647 (D) 3125 −0.58 TGN-S-S-SEQ ID NO: 1647 (D) 625 −0.59 TGN-S-S-SEQ ID NO: 1647 (D) 125 −0.52 Note: Every amino acid (except glycine) can occur in two isomeric forms, because of the possibility of forming two different enantiomers (stereoisomers) around the central carbon atom. By convention, these are called L- and D-forms, analogous to left-handed and right-handed configurations.

In Vivo Assay—In Vivo Evaluation in Mice:

Female CD-1 mice (Charles River) were injected in accordance with either a sequential dosing paradigm or a co-dosing paradigm. In the sequential dosing paradigm, the targeted siRNA (SCE) is dosed at t=0 and the targeted peptide is separately dosed up to 2 hr before the SCE (−2 hr) or up to 24 hr after the SCE (+24 hr). In the co-dosing paradigm, the SCE and peptides are co-formulated and dosed together in the same formulation as a single injection at t=0. The mice were dosed either by intravenous (i.v.) or subcutaneous (s.c.) injection of SCE and peptide. For the i.v. doses, the compounds were injected into the tail vein of the mice. For the s.c. doses, the compounds were injected in the subcutaneous space on the back of the mouse between the shoulder blades. At the indicated harvest times (measured from t=0 when the siRNA was dosed, regardless of when the peptide was dosed), the animals were sacrificed and 3 mm liver punches were collected, preserved in RNAlater (Ambion), and stored at 4° C. Separate 5 mm liver punches were collected, placed in 96-well plates, frozen on dry ice, and stored at −80° C. until use.

mRNA Knockdown Measurement:

The 3 mm liver punches were removed from RNAlater and homogenized in Trizol (Invitrogen) using a bead mill tissue lyser (Qiagen); disruption was performed for two 5-minute cycles at 30 Hz. RNA extraction was performed using 1-bromo-2-chloropropane (Acros Organics) and total RNA was isolated from the aqueous phase using the MagMax RNA isolation method (Ambion). RNA (125 ng) was reverse transcribed using the High Capacity cDNA Reverse Transcription kit (Applied Biosystems). TaqMan qPCR analysis was performed with an ABI 7900 Real-Time PCR System using TaqMan Fast Advanced Master Mix (Applied Biosystems). All TaqMan probes and primers for CTNNB1 and PPIB (housekeeping gene) were purchased from Applied Biosystems as pre-validated gene expression assays. Results are calculated by the comparative Ct method, where the difference between the CTNNB1 Ct value and the PPIB Ct value (ΔCt) is calculated and then further normalized relative to the PBS control by taking a second difference (ΔΔCt), as described previously (1).

Table-3, shows the mRNA knockdown data of multiple peptide conjugates dosed sequentially with peptide dosed 15 min after siRNA via intravenous (IV) route

Stem-Loop qPCR:

The same liver homogenates used to measure mRNA knockdown were also used to measure the concentration of CTNNB1 siRNA in the liver using a modified quantitative stem-loop RT-PCR protocol (2). Liver homogenate samples were diluted in TE buffer and then the antisense strand of the siRNA (5′-UUUCGAAUCAAUCCAACAGUU-3′; Seq. ID No. 1810) was reverse transcribed with 25 nM of a CTNNB1-specific stem-loop primer (5′-GTCGTATCCAGTGCAGGGTCCGAGGTATTCGCACTGGATACGACAACTGTTG-3′; Seq. ID No. 1811) using a TaqMan MicroRNA reverse transcription kit (Applied Biosystems) using 0.5 μL MultiScribe RT enzyme per reaction. A standard curve was generated by spiking CTNNB1 siRNA into untreated liver homogenate and then serially diluting with TE buffer. The cDNA from the RT step was utilized for real-time PCR using TaqMan Universal Master Mix (Applied Biosystems) with 1.5 μM of forward primer (5′-GGCGG CTTTCGAATCAATCCA-3′; Seq. ID No. 1812), 0.75 μM of reverse primer (5′-AGTGCAGGGTCCGAG-3′; Seq. ID No. 1813), and 0.2 μM of probe (5′-6FAM-TGGATACGACAACTGTTG-3′; Seq. ID No. 1814). Quantitative PCR reactions were performed using standard cycling conditions in an ABI 7900HT Fast Real-Time PCR System. Normalized Ct values were transformed into plasma concentrations using the linear equation derived from the standard curve.

Quantitation of siRNA Bound to RISC:

The 5 mm liver punches were homogenized in lysis buffer (50 mM Tris, 200 mM NaCl, 2 mM EDTA, 0.5% Triton-X-100, 1 mg/mL heparin, 1 tablet/50 mL of cOmplete EDTA-free protease inhibitor cocktail, and 200 U/mL benzonase), using a Geno/Grinder (SPEX SamplePrep Corp) with a stainless steel grinding ball ( 5/32″, 4 mm SPEX SamplePrep Corp) in a 96-well plate at 1100 strokes per minute for five intervals of one min each at 4° C. Samples were then centrifuged at 14,000 rpm for 30 min at 4° C. and protein levels were determined using a Peirce BCA Kit. Mouse anti mouse Ago2 monoclonal antibody (018-22021, Wako) was bound to magnetic beads (Invitrogen Dynabeads Protein G) in a 96-well microtiter plate. Liver lysates were incubated overnight at 4° C. with the antibody-magnetic bead complex. Post-incubation the samples were washed, incubated with 10 U/mL of benzonase (Sigma Aldrich) to reduce background, resuspended in 0.01% NP-40 detergent, and eluted off of the magnetic bead using heat (95° C. for 15 min). Using the 0.01% NP-40 samples, the antisense strand of the siRNA was quantitated using the stem-loop procedure described above, except that the standard curve was generated by spiking CTNNB siRNA into 0.01% NP-40 and then serially diluting with 0.01% NP-40. Simultaneously, the 0.01% NP-40 samples were used to quantitate miR-16 (5′-UAGCAGCACGUAAAUAUUGGCG-3′; Seq. ID No. 1815) using TaqMan MicroRNA Assay hsa-mir-16 (Applied Biosystems assay ID 000391) following the manufacturer's kit instructions. A standard curve was generated by spiking miR-16 into 0.01% NP-40 and then serially diluting with 0.01% NP-40. Quantitative PCR reactions were performed using standard cycling conditions in an ABI 7900HT Fast Real-Time PCR System. Normalized Ct values were transformed into liver concentrations using the linear equation derived from the standard curve. Using the concentrations derived from the standard curves of both the CTNNB1 siRNA and the miR-16, a ratio of RISC-bound siRNA to RISC-bound miR-16 was determined.

In Vivo Evaluation in Non-Human Primates:

Chair-trained rhesus monkeys were dosed with siRNA at t=0 by i.v. injection into the saphenous vein and then dosed with peptide (or sucrose buffer) by i.v. injection into the saphenous vein 15 min later. At indicated harvest times, monkeys were sedated using ketamine and/or telazol (5-30 mg/kg or 4-6 mg/kg, respectively) and then a ˜500 mg liver biopsy sample was obtained during a minimally invasive surgery (MIS) procedure. The liver tissue was stored in RNAlater and processed for mRNA knockdown as described above. The liver tissue was also processed for stem-loop qPCR and RISC binding as described above. The only differences were that rhesus-specific TaqMan probes and primers for CTNNB1 and PPM (housekeeping gene) were purchased from Applied Biosystems and that a mouse anti human Ago2 monoclonal antibody (018-22033, Wako) was used during the immunoprecipitation step in the RISC analysis

The structure of TGN-S-S-peptide is the same as that shown above for Table 5 and the structure of TGN-L-siRNA is shown below. The activity data is listed in Table 6.

TABLE 6 mRNA Knockdown Data - Sequential Dosing with Peptide Dosed 15 min After siRNA via Intravenous (IV) Route Targeted siRNA Targeted In vivo mRNA Targeted Targeted dose-IV peptide knockdown siRNA peptide (mg/kg) dose-IV (mg/kg) (%) siRNA-IV TGN-S-S-SEQ ID NO: 1710 (D) 5 2 66 siRNA-IV TGN-S-S-SEQ ID NO: 1710 (D) 5 10  79 siRNA-IV TGN-S-S-SEQ ID NO: 1710 (D) 2 2 58 siRNA-IV TGN-S-S-SEQ ID NO: 1710 (D) 2 10  64 siRNA-IV TGN-S-S-SEQ ID NO: 1710 (D) 0.5 2 30 siRNA-IV TGN-S-S-SEQ ID NO: 1710 (D) 0.5 10  67 siRNA-IV — 5 0 35 siRNA-IV — 2 0 25 siRNA-IV — 0.5 0 25 TGN-L-siRNA-III — 0.5 0 30 TGN-L-siRNA-III — 0.25 0 15 TGN-LsiRNA-III TGN-S-S-SEQ ID NO: 1710 (D) 0.5 25  63 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1710 (D) 0.5 18  68 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1710 (D) 0.25 10  69 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1710 (D) 0.25 5 50 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1643 (D) 0.25 10  41 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1078 (D) 0.25 10  53 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1662 (D) 0.25 10  32 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1696 (D) 0.25 10  44 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1657 (D) 0.25 10  35 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1660 (D) 0.25 10  34 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1654 (D) 0.25 2 51 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1654 (D) 0.25 10  72 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1654 (D) 0.25 50* 65 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1653 (D) 0.25 50  69 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1653 (D) 0.25 10  63 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1652 (D) 0.25 10  37 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1651 (D) 0.25 10  49 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1650 (D) 0.25 10  49 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1649 (D) 0.25 10  41 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1648 (D) 0.25 10  41 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1647 (D) 0.25 10  29 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1701 (D) 0.25 2 57 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1701 (D) 0.25 10  68 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1701 (D) 0.25 25  77 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1701 (D) 0.25 50* 82 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1645 (D) 0.25 10  37 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1628 (D) 0.25 10* All mice died TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1633 (D) 0.25 10  55 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1632 (D) 0.25 10  36 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1634 (D) 0.25 10  17 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1631 (D) 0.25 10  17 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1697 (D) 0.25 10  52 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1702(D) 0.25 5 75 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1703 (D) 0.25 5 54 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1704 (D) 0.25 5 64 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1705 (D) 0.25 5 59 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1706 (D) 0.25 5 61 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1707 (D) 0.25 5 56 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1708 (L) 0.25 5 46 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1709 (L) 0.5 5 16 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1710 (L) 0.5 5 21 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1711 (L) 0.5 5 36 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1712 (L) 0.5 5 34 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1713 (L) 0.25 2 0 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1713 (L) 0.25 10  2 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1715 (L) 0.5 5 28 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1716 (L) 0.5 5 39 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1717(L) 0.5 5 16 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1718 (L) 0.25 10  6 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1719 (L) 0.25 5 25 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1403 (L) 0.25 2 22 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1403(L) 0.25 10  24 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1518(L) 0.25 2 18.3 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1518 (L) 0.25 10  13 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1517 (L) 0.25  2, 18 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1517 (L) 0.25 10  18 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1516 (L) 0.25 5 14 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 935 (L) 0.25 2 17 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 935 (L) 0.25 10  23 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1391 (L) 0.5 10  6 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1248 (L) 0.5 5 24 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1720 (L) 0.5 10  31 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1721 (L) 0.5 10  8 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1722 (L) 0.5 10  21 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1723 (L) 0.5 10  5 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1724 (L) 0.5 10  21 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1725 (L) 0.25 10  19 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1726(D) 0.25 10  23 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1727 (D) 0.25 10  26 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1728(D) 0.25 10  23 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1729 (L) 0.25 10  10 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1730 (D) 0.25 10  43 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1731(D) 0.25 10  30 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1732 (D) 0.25 5 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1733 (D) 0.25 5 73 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1734 (D) 0.25 5 61 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1732 (D) 0.25 5 35 TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 1733(D) 0.25 1 60 TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 1733(D) 0.25 3 75 TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 1733(D) 0.25 10  58 TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 1733(D) 0.25 50  50 TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 1738 (D) 0.25 1 25 TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 1738 (D) 0.25 3 44 TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 1740 (L) 0.25 3 20 TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 1741(L) 0.25 3 24 TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 1740 (D) 0.25 1 23 TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 1740 (D) 0.25 3 42 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1709 (D) 0.25 2 54 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1709 (D) 0.25 10  65 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1709 (D) 0.25 25  77 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1709 (D) 0.25 35  81 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1744 (D) 0.5 2 28 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1744 (D) 0.5 10  33 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1745 (D) 0.5 2 54 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1745 (D) 0.5 10  69 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1745 (D) 0.5 25  66 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1746 (D) 0.5 2 31 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1746 (D) 0.5 10  25 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1489 (D) 0.5 2 37 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1489 (D) 0.5 10  26 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1489 (D) 0.5 25  34 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1419 (D) 0.5 2 43 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1419 (D) 0.5 10  78 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1419 (D) 0.5 25* 76 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1248 (D) 0.5 2 42 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1248 (D) 0.5 10  74 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 1248 (D) 0.5 25* 58 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 26 (D) 0.5   0.5 26 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 26 (D) 0.5 2 40 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 26 (D) 0.5 5 65 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 26 (D) 0.5 10  70 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 74 (D) 0.5   0.5 26 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 74 (D) 0.5 2 44 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 74 (D) 0.5 5 51 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 74 (D) 0.5 10  68 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 82 (D) 0.5   0.5 40 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 82 (D) 0.5 2 42 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 82 (D) 0.5 5 50 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 82 (D) 0.5 10  60 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 543 (D) 0.5   0.5 35 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 543 (D) 0.5 2 60 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 543 (D) 0.5 5 65 TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 543 (D) 0.5 10  75 TGN-L-siRNA-I — 0.5 0 20 TGN-L-siRNA-I 2K-PEG-S-S-Seq-ID-50 (D) 0.5   0.5 22 TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 26 (D) 0.5 2 25 TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 26 (D) 0.5 5 45 TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 26 (D) 0.5 10  45 TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 74 (D) 0.5   0.5 20 TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 74 (D) 0.5 2 20 TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 74 (D) 0.5 5 20 TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 74 (D) 0.5 10  20 TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 82 (D) 0.5 2 15 TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 82 (D) 0.5 5 30 TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 82 (D) 0.5 10  45 TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 1710 0.5 2 25 (D) TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 1710 0.5 5 15 (D) TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 1710 0.5 10  25 (D) TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 543 (D) 0.5 2 25 TGN-L-siRNA-I 2K-PEG-S-S-SEQ ID NO: 543 (D) 0.5 5 25 Note: D—D isomer of peptide; L—L isomer of peptide; 2K-S-S-PEG-SEQ ID NO = 2K-PEG-S-S-peptide; *lethal at this dose Comparison of Sequential Dosing (Peptide Dosed 15 Min after siRNA) Vs. Co-Dosing and Comparison of SC Vs. IV Dosing

The structure of TGN-S-S-peptide is the same as that shown above for Table 5 and the structure of TGN-L-siRNA is the same as that shown above for Table 6. The activity data is listed in Table 7.

TABLE 7 (i) Comparison of sequential dosing (peptide dosed 15 min after siRNA) vs. co-dosing (ii) Comparison of s.c. vs. i.v. dosing In vivo Targeted Targeted mRNA Targeted siRNA dose peptide dose knockdown Route of siRNA Targeted peptide (mg/kg) (mg/kg) (%) administration TGN-L-siRNA-III 0.5 0 40 IV TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 2 30 Sequential dosing-IV 26 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 5 60 Sequential dosing-IV 26 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 10 70 Sequential dosing-IV 26 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 2 30 Sequential dosing-SC 26 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 5 25 Sequential dosing-SC 26 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 10 25 Sequential dosing-SC 26 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 2 60 Sequential dosing-IV 1710 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 5 66 Sequential dosing-IV 1710 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 10 75 Sequential dosing-IV 1710 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 2 65 Sequential dosing-SC 1710 (D) TGN-L-siRNA-III TGN-S-SSEQ ID NO: 0.5 5 64 Sequential dosing-SC 1710(D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 10 66 Sequential dosing-SC 1710 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 2 30 Co-dosing-IV 26 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 5 60 Co-dosing-IV 26 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 10 70 Co-dosing-IV 26 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 2 30 Co-dosing-SC 26 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 5 25 Co-dosing-SC 26 (D) TGN-L-siRNA-III TGN-S-S-SEQ ID NO: 0.5 10 25 Co-dosing-SC 26 (D) TGN-L-siRNA-II — 0.5 0 25 SC TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 0.5 2 66 Co-dosing-SC 1709 (D) TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 0.5 10 77 Co-dosing-SC 1709 (D) TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 0.5 2 54 Sequential dosing-SC 1709 (D) TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 0.5 10 72 Sequential dosing-SC 1709 (D) TGN-L-siRNA-II — 0.25 0 25 IV TGN-L-siRNA-II — 0.25 0 9 SC TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 0.25 3 69 Sequential dosing-IV 1733 (D) TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 0.25 10 58 Sequential dosing-IV 1733 (D) TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 0.25 3 47 Sequential dosing-SC 1733 (D) TGN-L-siRNA-II TGN-S-S-SEQ ID NO: 0.25 10 67 Sequential dosing-SC 1733 (D) Note: D—D isomer of peptide. Comparison of Disulfide Vs. ECL Vs. CDM Linkages Between Targeting Ligand and Peptide

The structure of TGN-S-S-peptide is the same as that shown above for Table 5 and the structure of TGN-L-siRNA is the same as that shown above for Table 6. The activity data is listed in Table 8.

TABLE 8 Comparison of Disulfide vs. ECL vs. CDM Linkages between Targeting Ligand and Peptide Targeted Targeted In vivo mRNA Targeted siRNA dose peptide dose knockdown siRNA Targeted peptide (mg/kg) (mg/kg) (%) Peptide sequence TGN-L- TGN-S-S-SEQ ID 0.25 3 46.1 cglfgeieelieeglenlidwgng siRNA-II NO: 1745 (D) TGN-L- TGN-S-S-SEQ ID 0.25 1 44.4 cglfgeieelieeglenlidwgng siRNA-II NO: 1745 (D) TGN-L- TGN-ECL-SEQ ID 0.25 3 47.4 glfgeieelieeglenlidwgng siRNA-II NO: 1801 (D) TGN-L- TGN-ECL-SEQ ID 0.25 1 29.6 glfgeieelieeglenlidwgng siRNA-II NO: 1801 (D) TGN-L- TGN-CDM-SEQ ID 0.25 3 24.9 glfgeieelieeglenlidwgng siRNA-II NO: 1801 (D) TGN-L- TGN-CDM-SEQ ID 0.25 1 23.0 glfgeieelieeglenlidwgng siRNA-II NO: 1801 (D) TGN-L- TGN-S-S-SEQ ID 0.25 3 33.9 cffgaiwefihsil siRNA-II NO: 74 (D) TGN-L- TGN-S-S-SEQ ID 0.25 1 15.8 cffgaiwefihsil siRNA-II NO: 74 (D) TGN-L- TGN-ECL-SEQ ID 0.25 3 64.0 gffgaiwefihsil siRNA-II NO: 1802 (D) TGN-L- TGN-ECL-SEQ ID 0.25 1 28.7 gffgaiwefihsil siRNA-II NO: 1802 (D)

One skilled in the art would readily appreciate that the present invention is well adapted to carry out the objects and obtain the ends and advantages mentioned, as well as those inherent therein. The methods and compositions described herein, as presently representative of preferred embodiments, are exemplary and are not intended as limitations on the scope of the invention. Changes therein and other uses will occur to those skilled in the art, which are encompassed within the spirit of the invention, are defined by the scope of the claims. 

1. A method for inhibiting expression of a gene of a subject comprising administering: (1) a composition comprising R-(L)_(a)-(G)_(b) to the subject; wherein: R is an oligonucleotide selected from the group consisting of DNA, RNA, siRNA, and microRNA; L is a linker and each occurance of L is independently selected from Table 3; G is a targeting ligand and each occurance of G is independently selected from Table 4; and each of a and b is independently 0, 1, 2, 3 or 4; and (2) a composition comprising (P)_(c)-(L)_(d)-(G)_(e) to the subject; wherein: P is a peptide and each occurance of P is independently selected from Table 2; L is a linker and each occurance of L is independently selected from Table 3; G is a targeting ligand and each occurance of G is independently selected from Table 4; d is 0, 1, 2, 3, 4, 5 or 6; and each of c and e is independently 1, 2, 3, 4, 5 or
 6. 2. The method of claim 1, wherein R is a ds siRNA or ss siRNA.
 3. The method of claim 1, wherein each occurance of P is independently selected from Table 2b.
 4. The method of claim 1, wherein each occurance of L is independently selected from Table 3a.
 5. The method of claim 1, wherein each occurance of G is independently selected from Table 4a.
 6. The method of claim 5, wherein G is a ligand of the following formula:


7. The method of claim 1, wherein: each of a and b is independently 0, 1 or 2; c is 1 or 2; and each of d and e is independently 1, 2 or
 3. 8. The method of claim 1, comprising administering: (1) a composition comprising R-(L)_(a)-(G)_(b) to the subject; wherein: R is an siRNA; L is a linker and each occurance of L is independently selected from Table 3a; G is a targeting ligand and each occurance of G is independently selected from Table 4a; and each of a and b is independently 0, 1 or 2; and (2) a composition comprising (P)_(c)-(L)_(d)-(G)_(e) to the subject; wherein: P is a peptide and each occurance of P is independently selected from Table 2b; L is a linker and each occurance of L is independently selected from Table 3a; G is a targeting ligand and each occurance of G is independently selected from Table 4a; and each of c, d and e is independently 1, 2 or
 3. 9. The method of claim 8, wherein: L of R-(L)_(a)-(G)_(b) is selected from

wherein m is an integer selected from 0 to 10; G of R-(L)_(a)-(G)_(b) is:

and (P)_(c)-(L)_(d)-(G)_(e) of composition (2) is:

wherein P is a peptide selected from Table 2b; and wherein L of composition (2) is selected from:

wherein m is an integer selected from 0 to 10,


10. The method of claim 9, wherein each L of compositions (1) and (2) is independently


11. The method of claim 1, wherein: the composition comprising R-(L)_(a)-(G)_(b) and the composition comprising (P)_(c)-(L)_(d)-(G)_(e) are co-administered at the same time.
 12. The method of claim 1, wherein: the composition comprising R-(L)_(a)-(G)_(b) and the composition comprising (P)_(c)-(L)_(d)-(G)_(e) are sequentially administered about 0.1 to 1 hour apart.
 13. The method of claim 1, wherein the oligonucleotide is administered at a dose of 0.1 to 5 mpk; and the peptide is administered at a dose of 1 to 100 mpk.
 14. A composition for dual molecular delivery of an oligonucleotide and a peptide conjugate comprising: (1) R-(L)_(a)-(G)_(b); and (2) (P)_(c)-(L)_(d)-(G)_(e); wherein: R is an oligonucleotide selected from the group consisting of DNA, RNA, siRNA, and microRNA; P is a peptide and each occurance of P is independently selected from Table 2; L is a linker and each occurance of L is independently selected from Table 3; G is a targeting ligand and each occurance of G is independently selected from Table 4; each of a and b is independently 0, 1, 2, 3 or 4; and each of c, d and e is independently 1, 2, 3, 4, 5 or
 6. 15. The composition of claim 14, wherein: R is an siRNA; each occurance of P is independently selected from Table 2b; each occurance of L is independently selected from Table 3a; each occurance of G is independently selected from Table 4a; each of a and b is independently 0, 1 or 2; c is 1 or 2; and each of d and e is independently 1, 2 or
 3. 16. The composition of claim 14, wherein Y comprises a ligand of the following formula:


17. The composition of claim 14, wherein each of a and b is independently 0 or 1; c is 1; and each of d and e is an
 1. 18. The composition of claim 14, wherein: (1) G of R-(L)_(a)-(G)_(b) is:

and each of a and b is 1; and (2) (P)_(c)-(L)_(d)-(G)_(e) is:

wherein P is a peptide selected from Table 2b; and wherein each L of compositions (1) and (2) is independently selected from:


19. The composition of claim 14, wherein R-(L)_(a)-(G)_(b) further comprises a lipid and/or solubilizing agent.
 20. The composition of claim 14, wherein: the oligonucleotide is a double stranded siRNA; and G is attached to the guide strand or the passenger strand of the siRNA at different 2′-position of the ribose rings and/or at different terminal 3′ and/or 5′-positions. 